Polymer Loading Research Articles

Titanium Dioxide-Decorated and Silanized Electrospun Recycled Polyethylene Terephthalate (PET) Fibers for Filtration

Abstract Electrospinning methods have produced polymer-based non-woven fibers that have excellent filtration for use as air filter media, however most work have been focused on producing thinner fibers by reducing polymer loading. In this work, polyethylene terephthalate (PET) plastic from used soda plastic bottles was electrospun and decorated with nano-TiO2 to produce nonwoven media with antimicrobial properties. Electrospinning parameters were optimized to maintain higher loading percentage of PET to as much as 30% (w/v) with resulting fibers having an average diameter of 1.8 μm. Electrospun fiber mats were then treated with a silane-based binder for surface-decoration with nano-TiO2 coating to impart antimicrobial properties to these fibers. XRF mapping showed uniform coating of the nanoparticles. Atomic ratios from XRF of Ti to Si did not significantly change before and after ultrasonication washing signifying the covalent coating of the nanoparticles onto the fiber matrix.

Preliminary Insight Into Torsion of Additively-Manufactured Polylactic Acid (PLA)-Based Polymers

BackgroundPolymers in practical applications often face diverse torsional loads, such as polymeric gears, couplings, scaffolds, etc. Meanwhile, additive manufacturing enables the creation of intricate geometries for specific needs and its application to fabricate various component parts has grown exponentially. Nevertheless, research on cyclic and reversed cyclic torsional loading of additively-manufactured polymers is very limited.ObjectiveMechanical characterization of monotonic, cyclic, and reversed cyclic torsion in polylactic acid (PLA), PLA Premium, and PLA Tough materials.MethodsSpecimens were 3D-printed with a 0° build orientation using an extrusion technique and two infill orientation angles (± 45° and 0°/90°). Specimens were subjected to underwent monotonic, cyclic, and reversed cyclic torsion until failure.ResultsRegardless of material type, ductile fracture governed the behavior under monotonic loading and brittle failure under cyclic and reversed cyclic loadings. Specimens with a ± 45° infill orientation outperformed their 0°/90° counterparts across all materials, with PLA Premium exhibiting superior performance compared to PLA and PLA Tough. Importantly, it was demonstrated that the previously-proposed multilinear idealized shear stress-shear strain curve, developed for monotonic loading of 15 different polymers, also applies to the envelope curves of cyclic and reversed cyclic loading in PLA-based polymers. Thus, it is useful as material model input for numerical simulation purposes.

Best of Both Worlds: Adsorptive Ultrafiltration Nanocellulose‐Hypercrosslinked Polymer Hybrid Membranes for Metal Ion Removal

Efficient water treatment ideally combines ion exchange for the removal of hardness elements and toxic trace metals as well as ultrafiltration for the removal of particulate matter. Although promising for adsorption, many high‐surface‐area polymer materials cannot be easily processed into freestanding membranes or packed bed columns, due to poor solution processability and high back pressures, respectively. The preparation of hybrid membranes comprising sulfonated hypercrosslinked polymers entrapped in nanocellulose papers is described. The hybrid membranes are effective for simultaneous ultrafiltration and ion exchange. Increasing the polymer loading of the hybrid membrane produces synergy by increasing the permeance of the membranes while enhancing the ion adsorption capacity to values exceeding those of bulk hypercrosslinked polymers. The maximum ion adsorption capacity for copper is determined to be ≈100 mg g−1 outperforming that of pure polymer (71 mg g−1) and commercially available ion exchange resins. Competitive adsorption is tested in samples containing water hardness elements and trace toxic metal ions showing high ion‐exchange capacities. Even when fully loaded with water hardness elements, Ba2+ and Sr2+ are still removed from solution.

Connecting rate-dependent loading and relaxation behaviors of glassy polymers by fractional models

Connecting rate-dependent loading and relaxation behaviors of glassy polymers by fractional models

Design of electrical energy harvesting devices utilizing air bubbles sliding along a fluoropolymer immersed in water

Recent research has shown that it is possible to utilize contact electrification combined with electrostatic induction to harvest electrical energy from the mechanical motion of air bubbles sliding along a charged solid surface immersed in water. The working principle of these devices is simple, but the design is usually complicated as transduction efficiency depends on a number of interdependent parameters. Here we propose a simple analytical model and demonstrate how it can be used to determine the optimal energy per bubble for a given resistive load. The model allows one to estimate the optimal energy harvested per bubble in terms of polymer thickness, electrode separation and load resistance. It is shown that the model provides a good fit to experimental data. The model may be used as an initial step when designing energy harvesting devices utilizing air bubbles sliding along a solid surface.

Open-Air Chemical Recycling: Fully Oxygen-Tolerant ATRP Depolymerization.

While oxygen-tolerant strategies have been overwhelmingly developed for controlled radical polymerizations, the low radical concentrations typically required for high monomer recovery render oxygen-tolerant solution depolymerizations particularly challenging. Here, an open-air atom transfer radical polymerization (ATRP) depolymerization is presented, whereby a small amount of a volatile cosolvent is introduced as a means to thoroughly remove oxygen. Ultrafast depolymerization (i.e., 2 min) could efficiently proceed in an open vessel, allowing a very high monomer retrieval to be achieved (i.e., ∼91% depolymerization efficiency), on par with that of the fully deoxygenated analogue. Oxygen probe studies combined with detailed depolymerization kinetics revealed the importance of the low-boiling point cosolvent in removing oxygen prior to the reaction, thus facilitating effective open-air depolymerization. The versatility of the methodology was demonstrated by performing reactions with a range of different ligands and at high polymer loadings (1 M monomer repeat unit concentration) without significantly compromising the yield. This approach provides a fully oxygen-tolerant, facile, and efficient route to chemically recycle ATRP-synthesized polymers, enabling exciting new applications.

Reduction of Z alpha-1 antitrypsin polymers in human iPSC-hepatocytes and mice by LRRK2 inhibitors.

Alpha-1 antitrypsin deficiency (A1ATD) is a life-threatening condition caused by inheritance of the SERPINA1 'Z' genetic variant (PiZ) driving AAT protein misfolding in hepatocytes. There remain no approved medicines for this disease. Here, we report the results of a small molecule screen performed in patient derived iPSC-hepatocytes that identified Leucine-rich repeat kinase-2 (LRRK2) as a potentially new therapeutic target. Of the commercially available LRRK2 inhibitors tested, we identified CZC-25146, a candidate with favorable pharmacokinetic properties, as being capable of reducing polymer load, increasing normal AAT secretion, and reducing inflammatory cytokines in both cells and PiZ mice. Mechanistically, this effect was achieved through induction of autophagy. Our findings support the use of CZC-25146 and LRRK2 inhibitors in hepatic proteinopathy research and their further investigation as novel therapeutic candidates for A1ATD.

Effect of Water-Soluble Polymers on the Rheology and Microstructure of Polymer-Modified Geopolymer Glass-Ceramics.

This work explores the effects of rigid (0.1, 0.25, and 0.5 wt. %) and semi-flexible (0.5, 1.0, and 2.5 wt. %) all-aromatic polyelectrolyte reinforcements as rheological and morphological modifiers for preparing phosphate geopolymer glass-ceramic composites. Polymer-modified aluminosilicate-phosphate geopolymer resins were prepared by high-shear mixing of a metakaolin powder with 9M phosphoric acid and two all-aromatic, sulfonated polyamides. Polymer loadings between 0.5-2.5 wt. % exhibited gel-like behavior and an increase in the modulus of the geopolymer resin as a function of polymer concentration. The incorporation of a 0.5 wt. % rigid polymer resulted in a three-fold increase in viscosity relative to the control phosphate geopolymer resin. Hardening, dehydration, and crystallization of the geopolymer resins to glass-ceramics was achieved through mold casting, curing at 80 °C for 24 h, and a final heat treatment up to 260 °C. Scanning electron microscopy revealed a decrease in microstructure porosity in the range of 0.78 μm to 0.31 μm for geopolymer plaques containing loadings of 0.5 wt. % rigid polymer. Nano-porosity values of the composites were measured between 10-40 nm using nitrogen adsorption (Brunauer-Emmett-Teller method) and transmission electron microscopy. Nanoindentation studies revealed geopolymer composites with Young's modulus values of 15-24 GPa and hardness values of 1-2 GPa, suggesting an increase in modulus and hardness with polymer incorporation. Additional structural and chemical analyses were performed via thermal gravimetric analysis, Fourier transform infrared radiation, X-ray diffraction, and energy dispersive spectroscopy. This work provides a fundamental understanding of the processing, microstructure, and mechanical behavior of water-soluble, high-performance polyelectrolyte-reinforced geopolymer composites.

3D macroporous MXene/sodium alginate aerogels with “brick-concrete” structures for highly efficient solar-driven water purification

Interfacial water evaporation, powered by solar energy, holds great promise to extract freshwater from seawater on a global scale. It has the potential to address the world's water scarcity challenges using renewable energy. While the ideal design of evaporator materials is critical to the interfacial vaporization desalination, tailoring the structures and compositions of solar evaporators and figuring out the structure/composition-performance relationship of evaporators remains unexplored. Herein, 3D macroporous “brick-concrete” MXene/sodium alginate aerogel (MSA) evaporators were designed and fabricated with constant MXene content and varying polymer loading. The as-made MSAs show sodium alginate-dependent evaporating performance with an optimum evaporation rate of 3.28 kg m−2 h−1 (1 sun). This exceptional rate is attributed to several factors, including enhanced light absorption, optimized pore sizes, reduced enthalpy of evaporation and improved water transport. The water molecule states and hydrogen bonding network in the aerogels can be tuned by their compositions, resulting in the reduced evaporation enthalpy, the monolithic structures with controlled thermal conductivity facilitate the exploitation of environmental energy, leading to the high evaporation rate. Our study not only establishes design principles for achieving superior evaporation performance, but also sheds light on the relationship between structures, compositions, and performance of solar evaporators.

Hydraulic conductivity of bentonite-polymer geosynthetic clay liners to aggressive solid waste leachates

Hydraulic conductivity of conventional mock sodium bentonite (Na–B) and bentonite-polymer (B–P) geosynthetic clay liners (GCLs) were evaluated with three synthetic leachates that are chemically representative of aggressive leachates from coal combustion product (CCR) (I = 3179 mM), mining waste (MW) (I = 2127 mM, pH = 2.0), and municipal solid waste incineration ash landfill (MSWI) (I = 2590 mM). The mock B–P GCLs were created by dry mixing bentonite with branched, linear, or crosslinked polymer. The polymer loading of mock B–P GCLs ranged from 3 to 15%. Comparative tests were also conducted with Na–B GCLs. The mock Na–B GCLs cannot maintain low hydraulic conductivity to aggressive CCR, MW, and MSWI leachates. Mock B–P GCLs with 10% branched polymer had low hydraulic conductivity (< 1.0 × 10−10 m/s) to synthetic MW and MSWI leachates at 20 kPa effective confining stress, whereas the hydraulic conductivity of mock B–P GCLs with 10% linear or crosslinked polymer ranged from 1.5 × 10−9 to 1.4 × 10−7 m/s. As the effective stress increased, the B–P GCLs branched polymer showed a faster decreasing trend than that of Na–B and B–P GCLs with linear or crosslinked polymer.

Polymer blending and nanophotocatalyst loading synergy in visible light‐driven photocatalytic PES/SPSf mixed matrix membranes

AbstractThe synergy of polymer blending and loading photocatalytic titania–amorphous carbon nanotubes (TiO2–aCNT) in tailoring the morphological, surface, and optoelectrical properties of membranes is investigated. High energy band gap (Eg) polyethersulfone (PES), and low Eg sulfonated polyethersulfone (SPSf) polymer blends were loaded with TiO2–aCNT nanocomposite fillers. SEM reveals membranes consisting of a selective layer, a dense sublayer and a spongy layer with the latter two consisting of a network of nanofibers whose diameters decrease with increasing TiO2–aCNT loading. The downshifting in the wavenumbers of sulfonyl and sulfone peaks in Fourier transform infrared and Raman spectra confirms bonding of TiO2–aCNT with PES/SPSf via these groups. Blending PES with SPSf decreases the Eg of the membranes while loading TiO2–aCNT produces a second band edge corresponding to = 2.8 eV. Suppression of charge recombination in membranes is realized at 1.2 filler wt.%. Charge separation occurrs via shuttling of the positive holes to the aCNTs and valence band of TiO2 while electrons are shuttled to the conduction bands of PES and SPSf. Electron impedance spectroscopy shows TiO2–aCNT loading reduces polymer membrane resistance to charge transport. Dye degradation up to 85% is realized under direct sunlight irradiation accompanied by mineralization.

Experimental Study on Flexural Behavior of RC Piles with Basalt Fiber-Reinforced Polymer Bars and Load Carrying Capacity Calculation

The practical application of BFRPB (Basalt Fiber-Reinforced Polymer Bars) as a support structure in foundation pit and slope engineering is relatively under-researched. The indoor tensile test presented in this paper is carried out on the bond between BFRPB and different labelled concrete. The mechanical characteristics of BFRPB, the failure characteristics, and the load-carrying capacity were analyzed. The results of this study demonstrate that the normal section stress of concrete cylindrical components with BFRP has a good linear relationship and supports the rationality of the flat section assumption. In circular reinforced concrete BFRP structures, the failure of the pile load occurs in four phases, and the cracking load is in the range of 51% to 67% of the normal yield load. The main bars increase in strain with load but become attenuated in the compression zone. The deformation of the main bars increases with the load but becomes muted in the compression zone. Based on the method of calculating the load-carrying capacity of GFRP-reinforced RC piles and the normal limit load-carrying moment obtained from in-door tests, the bending moment correction coefficient in the calculation formula for the load-carrying capacity of BFRP-reinforced RC piles was then obtained.

Molecular Weight-Independent "Polysoap" Nanostructure Characterized via In Situ Resonant Soft X-ray Scattering.

Studying polymer micelle structure and loading dynamics under environmental conditions is critical for nanocarrier applications but challenging due to a lack of in situ nanoprobes. Here, the structure and loading of amphiphilic polyelectrolyte copolymer micelles, formed by 2-acrylamido-2-methylpropanesulfonic acid (AMPS) and n-dodecyl acrylamide (DDAM), were investigated using a multimodal approach centered around in situ resonant soft X-ray scattering (RSoXS). We observe aqueous micelles formed from polymers of wide-ranging molecular weights and aqueous concentrations. Despite no measurable critical micelle concentration (CMC), structural analyses point toward multimeric structures for most molecular weights, with the lowest molecular weight micelles containing mixed coronas and forming loose micelle clusters that enhance hydrocarbon uptake. The sizes of the micelle substructures are independent of both the concentration and molecular weight. Combining these results with a measured molecular weight-invariant surface charge and zeta potential strengthens the link between the nanoparticle size and ionic charge in solution that governs the polysoap micelle structure. Such control would be critical for nanocarrier applications, such as drug delivery and water remediation.

Cyclic Thermomechanical Loading of Epoxy Polymer: Modeling with Consideration of Stress Accumulation and Experimental Verification.

Developing a viscoelastic model for the cyclic thermomechanical loading of thermosetting polymers is the main goal of this study. The model includes memory for residual thermal stresses and can consider stress accumulation across many loading cycles. By considering stress accumulation, we can improve predictions and understand how thermosetting polymers' stress-strain state changes under cyclic thermomechanical loading. This approach was validated through experimental verification to ensure its applicability in practical engineering scenarios. The experiment showed that the thermosetting polymer can accumulate stress during cycles of heating and mechanical loading during use. The results of the modeling and experiment are compared. The results have led to corrections in the way this model is applied to thermosetting polymers like the epoxy resin in this study. The corrected results matched well with the experimental measurements of stress under cyclic thermomechanical load, with a difference of only 1 to 6%.

Burst Release from In Situ Forming PLGA-Based Implants: 12 Effectors and Ways of Correction.

This systematic review examines the reasons for the phenomenon of active ingredient "burst" release, which is a major drawback of PLGA-based in situ formed implants, and the likely ways to correct this phenomenon to improve the quality of in situ formed implants with a poly(DL-lactide-co-glycolide) matrix. Actual and relevant publications in PubMed and Google Scholar databases were studied. The concept of the review was based on the theory developed during literature analysis of 12 effectors on burst release from in situ forming implants based on PLGA. Only those studies that sufficiently fully disclosed one or another component of the theory were included. The analysis resulted in development of a systematic approach called the "12 Factor System", which considers various constant and variable, endogenous and exogenous factors that can influence the nature of 'burst release' of active ingredients from PLGA polymer-based in situ formed implants. These factors include matrix porosity, polymer swelling, LA:GA ratio, PLGA end groups, polymer molecular weight, active ingredient structure, polymer concentration, polymer loading with active ingredients, polymer combination, use of co-solvents, addition of excipients, and change of dissolution conditions. This review also considered different types of kinetics of active ingredient release from in situ formed implants and the possibility of using the "burst release" phenomenon to modify the active ingredient release profile at the site of application of this dosage form.

Using viscosity as an index for polymer loading of bentonite-polymer composite geosynthetic clay liners

Bentonite-polymer composite (BPC) geosynthetic clay liners (GCLs) containing a mixture of air-dry granules of bentonite and polymer have been developed for containment of wastes that generate leachates that are too aggressive for conventional sodium bentonite GCLs. Sufficient polymer loading is essential for BPC GCLs to maintain low hydraulic conductivity, and expedient methods are needed for manufacturing quality control and construction quality control to confirm that BPC GCLs contain sufficient polymer. In this study, a methodology for developed to estimate the polymer loading based on viscosity testing of slurries prepared with the BPC. A simplified version of the method can be used to determine if polymer is present in a BPC. Factors influencing the viscosity measurement were evaluated systematically, including water-to-BPC ratio, tempering time, and mixing method. The method that was developed consists of (1) adding deionized water to dry BPCs to achieve a water-to-BPC ratio of 30, (2) blending the BPC-water mixture with an overhead stirrer at 5000 rpm for 30 min to create a homogeneous slurry, (3) tempering the slurry in a zip-top bag for 24 hr, and (4) measuring the viscosity of the slurry in a viscometer at 300 and 600 rpm. Linear relationships were developed between polymer loading and viscosity for two BPC GCLs. Independent validation confirmed that the polymer loading estimated with the method is ±0.25% of the actual polymer loading.

High energy-capacity and multiresponsive phase change fibers via in situ polymer composition with expanded carbon nanotube networks

Phase change fibers with abilities to storage/release thermal energy and response to multiple stimuli are of high interest for wearable thermal management textiles. However, there are long-term challenges for carbon nanotube (CNT) network-directed phase change composites, such as the limited polymer loading, nonuniform composite structure, and weak connectivity between CNTs. Herein, an expansion-based in situ composition strategy is proposed to impregnate polyethylene glycol (PEG) into CNT network, leading to a high and homogeneous PEG loading (96 wt%) and robust PEG confinement inside the expanded CNT network. As the expansion induced CNT separation from aggregation, leading to the full utilization of CNT surfaces, the CNT/PEG composite fibers at the highest PEG loading exhibited superior high latent heat of 195–205 J g−1, and were electrically and thermally conductive. More importantly, owing to the confinement, these fibers showed remarkable cyclic thermal stability, without any liquid leakage. The composite fibers were also embroidered and woven into various fabrics, which showed excellent thermal managing capacity and rapid responses to electrical and optical stimuli.

Measurement of Magnetic Flux Density Changes in Mode I Interlaminar Fracture in Magnetostrictive Fiber–Embedded Glass Fiber-Reinforced Polymer Composites

As sensor materials for structural health monitoring (SHM, a nondestructive test for the continuous evaluation of the conditions of individual structural components and entire assemblies), magnetostrictive materials, piezoelectric materials, and optical fibers have attracted significant interest. In this study, the mode I interlaminar fracture load and crack self-detection potential of glass fiber-reinforced polymer (GFRP)–embedded magnetostrictive Fe–Co fibers were investigated via double cantilever beam testing. The results indicated that by controlling the amount of Fe–Co fibers introduced into GFRP, the number of Fe–Co fibers could be reduced without compromising the performance of GFRP. Furthermore, the magnetic flux density increased significantly with crack propagation, indicating that the magnetic flux density change could determine crack propagation.

The consequences of reduced anthropogenic activities during the COVID-19 pandemic on microplastic abundance in a tropical estuarine region: Goa, India

Plastic pollution is pervasive, as it has infiltrated every corner of the planet and the COVID-19 pandemic has caused a depletion in the production, consumption, and disposal of plastics. To find out the effect of the COVID-19 pandemic, a comparative assessment of microplastics (MPs) observed before and after the pandemic was evaluated in surface water and sediment from the major rivers of Goa, i.e. Mandovi and Zuari. To comprehend the relative difference in the abundance, characteristics, and source of MPs, samples were examined in both the dry and wet seasons. We found a sharp decrease in the concentration of MPs immediately after the isolated pandemic. During the dry and wet seasons, two to seven times less concentration of MPs was recorded for water and sediments after the pandemic period compared to the prior pandemic. MPs size, >300 μm were relatively abundant after the pandemic period in contrast to the prior pandemic (<300 μm sized MPs were more). Polyamide (PA), polyvinyl alcohol (PVAL), and polyvinyl chloride (PVC) were the dominant polymers after the pandemic whereas earlier the dominant polymers were polyacetylene, polyacrylamide (PAM), and polyvinyl pyrrolidone (PVP). The risk assessment of MPs in sediments (Polymer load index) was higher prior to the pandemic. The water quality parameters also indicated an improvement in the water quality during the pandemic. The present study clearly exhibited that due to the reduction of overall anthropogenic activities during the COVID-19 pandemic period, a sharp decline of plastic waste and MP abundance in the coastal water body in Goa, west coast of India was found. This study unveils the controlling factors (such as total solid waste generation, plastic waste, tourism activities, and the effect of monsoon) which influence the abundance and distribution of macro- and microplastics.

Polyphosphate-loaded silk fibroin membrane as hemostatic agent in oral surgery: a pilot study

PurposePost-interventional hemorrhage can result in serious complications, especially in patients with hemostatic disorders. Identification of safe and efficient local hemostatic agents is important, particularly in the context of an ageing society and the emergence of new oral anticoagulants. The aim of this in vitro study was to investigate the potential of silk fibroin membranes coated with the inorganic polymer polyphosphate (polyP) as a novel hemostatic device in oral surgery.MethodsCocoons of the silkworm Bombyx mori were degummed and dissolved. Varying amounts of long-chain polyP (2–2000 µg/mm2) were adsorbed to the surface of silk fibroin membranes. Analysis of the procoagulant effect of polyP-coated silk membranes was performed using real-time thrombin generation assays in human plasma. Increasing concentrations of polyP (0.15–500 µg/ml) served as a positive control, while uncoated silk fibroin membranes were used as negative control.ResultsPolyP-coated silk fibroin membranes triggered coagulation when compared to plasma samples and pure silk fibroin membranes. A polyP-dose-dependent effect of thrombin generation could be found with a maximum (ETP = 1525.7 nM⋅min, peak thrombin = 310.1 nM, time to peak = 9.8 min, lag time = 7.6 min.) at 200 µg/mm2 of polymer loading on the silk fibroin membrane surface.ConclusionsIn this study, it was demonstrated that silk fibroin membranes coated with polyP have the potential to act as a promising novel hemostatic device.Graphical