High Polymer Concentrations Research Articles

A comprehensive evaluation of the most-sold baby diapers on the market

The performance of baby diapers is highly related to the occurrence of diaper rash. However, a comprehensive evaluation of baby diapers on the market is unavailable. Herein, we systematically investigated the performance of the six most-sold baby diapers on the market. We disassembled the selected diapers and investigated the structure and properties of the main components, including the top sheet, acquisition sheet, absorbent core, and back sheet. Then the urine absorption capability, excrement spreading capability, run-off, and wetback of the diapers were investigated using urine and loose stool to reflect the functions of diapers in practical usage. Our results indicated that the performance of baby diapers is highly dependent on the structure and properties of each diaper component. Specifically, excrement run-off and wetback were highly related to excrement absorption speed and excrement spreading properties, respectively, which depend on the complex interactions among the top sheet, acquisition sheet, and absorbent core. In particular, designing the top sheet with a three-dimensional convex–concave structure or large holes was beneficial to fast excrement penetration. Meanwhile, employing an acquisition sheet could improve the excrement spreading properties. In addition, an absorbent core with a high content of super absorbent polymer and an absorption channel also contributed to a better excrement absorption property. Notably, Pampers and Moony diapers exhibited relatively low urine wetback. Bobdog and Babycare diapers showed 0 g urine run-off. Besides, Huggies, and Moony diapers were relatively soft, which could provide a better contact feeling during usage. Furthermore, Beaba diapers exhibited the best air permeability of 42.511 mm s−1 due to the existence of more breathable holes. Our study may provide scientific inspiration for researchers and enterprises to develop next-generation high-performance baby diapers and serve as a guideline for consumers to choose the right baby diapers.

Bioadhesive behaviors of HPMC E5: comparative analysis of various techniques, histological and human radiological evidence

Enhancing drug residence duration within the stomach offers distinct advantages for both localized and systemic effects. Numerous strategies have been proposed to extend drug residence time, with mucoadhesive polymers being a notable avenue. In this context, hydroxypropyl methylcellulose E5 has been employed as both a binding agent for granulating contrast metal powder and a mucoadhesive polymer, spanning various concentrations. The in vitro bioadhesion strength of the formulated tablets was gauged against the stomach lining of rabbits, for the quantification of bioadhesive forces. The temporal aspect of bioadhesion was evaluated through two approaches: one centered on gastric fluid dynamics and another proffered by the researchers, focusing on gastric wall kinetics. The results divulged a decline in bioadhesion force concomitant with high polymer concentrations. Histological examination of stained stomach sections revealed mucosal perturbations within the rabbit stomach. These disruptions exhibited an escalating trend in conjunction with elevated polymer concentrations, culminating in extensive disturbance at a 7.5% polymer concentration. The outcomes unveiled a direct relationship between polymer concentration increments and extended contact time. Subsequent radiological tracking of contrast metal behavior within a mature human stomach indicated a residence time of 6 h due to the entrapment of displaced components at disparate locations.

Segregative phase separation of strong polyelectrolyte complexes at high salt and high polymer concentrations.

The phase behavior of polyelectrolyte complexes and coacervates (PECs) at low salt concentrations has been well characterized, but their behavior at concentrations well above the binodal is not well understood. Here, we investigate the phase behavior of stoichiometric poly(styrene sulfonate)/poly(diallyldimethylammonium) mixtures at high salt and high polymer concentrations. Samples were prepared by direct mixing of PSS/PDADMA PECs, water, and salt (KBr). Phase separation was observed at salt concentrations approximately 1 M above the binodal. Characterization by thermogravimetric analysis, FTIR, and NMR revealed that both phases contained significant amounts of polymer, and that the polymer-rich phase was enriched in PSS, while the polymer-poor phase was enriched in PDADMA. These results suggest that high salt concentrations drive salting out of the more hydrophobic polyelectrolyte (PSS), consistent with behavior observed in weak polyelectrolyte systems. Interestingly, at the highest salt and polymer concentrations studied, the polymer-rich phase contained both PSS and PDADMA, suggesting that high salt concentrations can drive salting out of partially-neutralized complexes as well. Characterization of the behavior of PECs in the high concentration limit appears to be a fruitful avenue for deepening fundamental understanding of the molecular-scale factors driving phase separation in these systems.

Elaboration and rheological characterization of nanocomposite hydrogels containing C60 fullerene nanoplatelets.

Nanocomposite hydrogels were elaborated that consisted of a physical network formed by an amphiphilic polymer in which C60 fullerene nanoplatelets were embedded. Characterization showed that the nanoplatelets within the polymer network were aggregated. The presence of these nanoplatelets led to an increase of the shear modulus of the hydrogels, that cannot be explained by a filler effect alone. The nanocomposite gels displayed similar rheological behavior, both in linear and non-linear domains, as neat hydrogels at higher polymer concentrations. We suggest that the particles reinforced the gels by forming additional connections between the polymer chains.

Micro-mesoporous ferrierite obtained using the cationic polymer Luviquat and post-synthesis treatment

This study investigated for the first time the synthesis of ferrierite zeolite through the vapor-phase transport method using the cationic polymer Luviquat as a mesopores-generating agent, followed by desilication treatment. The effect of ferrierite's textural and acid properties was then evaluated in the catalytic cracking of ultra-high molecular weight polyethylene (UHMWPE). The synthesized zeolites showed a crystallinity of 91%–100% and similar Si/Al ratios. After the desilication, there was a decrease in these values along with an increase in acidity, attributable to the extraction of structural silicon. The strong interaction between the polymer and the zeolite precursor during the self-assembly process led to the formation of intracrystalline mesoporosity. However, an internal diffusion limit and/or steric hindrance hinders the complete incorporation of the polymer into the ferrierite structure, especially at high polymer concentrations. Thus, the optimal composition was 40% Luviquat, which resulted in twice the volume of mesopores compared to the sample prepared without the polymer. The desilication of the samples synthesized with the Luviquat led to a substantial increase in mesoporosity, ranging from 67% to 183%, relative to microporous ferrierite. The introduction of mesoporosity and the modification of acid properties in ferrierite contributed to a reduction in the temperature for the cracking of UHMWPE, between 66 and 93 °C compared to the pure polymer. However, in all cases, there was an increase in the average apparent activation energy in relation to desilicated microporous ferrierite zeolite, possibly due to changes in product distribution.

Characterizing a design space for a twin-screw wet granulation process: A case study of extended-release tablets

Twin-screw wet granulation is an emerging continuous manufacturing technology for solid oral dosage forms. This technology has been successfully employed for the commercial manufacture of immediate-released tablets. However, the higher polymer content in extended-release (ER) formulations may present challenges in developing and operating within a desired design space. The work described here used a systematic approach for defining the optimum design space by understanding the effects of the screw design, operating parameters, and their interactions on the critical characteristics of granules and ER tablets. The impacts of screw speed, powder feeding rate, and the number of kneading (KEs) and sizing elements on granules and tablets characteristics were investigated by employing a definitive screening design. A semi-mechanistic model was used to calculate the residence time distribution parameters and validated using the tracers. The results showed that an increase in screw speed decreased the mean residence time of the material within the barrel, while an increase in the powder feeding rate or number of KEs did the opposite and increased the barrel residence time. Screw design and operating parameters affected the flow and bulk characteristics of granules. The screw speed was the most significant factor impacting the tablet's breaking strength. The dissolution profiles revealed that granule characteristics mainly influenced the early phase of drug release. This study demonstrated that a simultaneous optimization of both operating and screw design parameters was beneficial in producing ER granules and tablets of desired performance characteristics while mitigating any failure risks, such as swelling during processing.

DEVELOPMENT OF CASTICIN-LOADED ETHYL CELLULOSE MICROPARTICLES BY SOLVENT EVAPORATION METHOD WITH SINGLE EMULSION SYSTEM

Objective: Casticin (Vitexicarpin) has shown immunoregulatory, antitumor, cytotoxicity, anti-inflammatory and analgesic properties. Application of the valuable bioactive compounds can be limited by their unpleasant taste, low bioavailability, volatilization of active compounds, sensitivity to the temperature, oxidation and UV light, as well as in vivo instability. The problem can be solved by coating the Casticin with a microencapsulation technique. The purpose of this research was to formulate the microcapsules of Casticin with solvent evaporation technique using Ethocel 10 cP. Methods: The microencapsulation process of Casticin was done by solvent evaporation technique (O/W: oil in water). The formula of Casticin microcapsules were designed into three formulas (Ethocel 10 cP: 10%, 15% and 20%). Microcapsules of Casticin were characterized for particle size, in terms of surface morphology by scanning electron microscope (SEM), encapsulation efficiency and release test. Results: In this research, the micoparticles containing Casticin has been developed by using ethyl cellulose (Ethocel 10 cP) as the polymer matrix. The results showed that high concentration of polymer (Ethocel 10 cP) used in microencapsulation resulted in better Casticin microcapsules in terms of physical characteristics. Particle size of microcapsules containing Casticin were in the range of 42.51 to 61.47 μm. Encapsulation efficiency (% EE) was categorized as good because the value were ≥ 80% to, which 91.57% to 96.24%. SEM picture of Casticin microcapsules revealed that the surface of microcapsule were a smooth surface and no pores of microcapsule were obtained. When Eudragit E100 used as a polymer, a rough and porous surface of microcapsule were obtained. Conclusion: It can be concluded that microcapsules of Casticin can be prepared by solvent evaporation method with a single emulsion system (O/W) using Ethocel 10 cP as polymer. Characterization of the microcapsules revealed that ethyl cellulose used on this method is applicable to produce microcapsules which stable in physical properties. A higher polymer concentration led to a more viscous solution, which delayed the polymer precipitation and resulted in a less porous polymer matrix with a slower drug release.

The role of the solvent nature in stretching polymer solutions (polyacrylonitrile spinning using different solvents)

We investigated how different solvents' affinity with polyacrylonitrile affects the formation of a jet that leads to stable fiber spinning. The study focused on two concentrations, one near and one above the crossover point where the topological entanglements are formed in the semi-dilute solutions. The role of the physical parameters of the solutions, including solvent-polymer affinity, viscosity, surface tension, and relaxation times, was analyzed. The experiment involved the uniaxial deformation of a solution drop under its weight, observed using a high-speed microscopic camera. The stability of the jet was associated with the relaxation time and solvent-polymer affinity. The continuous fiber spinning is mainly determined by the high enough polymer concentration in the solution, and the solvent nature, or by how the solution state is close to the theta conditions. Bicomponent mixed solvents offer two viable routes to achieve this – evaporating a more volatile component from the mixture to increase the polymer concentration, or modifying the solvent with a combination of solvents of different solvent quality. Both approaches have been experimentally validated, enabling the production of continuous stable fibers in the gel stretching regime. In this case, the jet stretching occurs under conditions Wi > 1. Thereby, the transition to the gel state promotes the necessary conditions for macromolecule orientation during fiber spinning.

Yield stress of in-situ polymerization modified cement paste

Achieving desired yield stress is crucial for various construction processes, especially in the emerging 3D concrete printing. In this paper, we present the possibility of enhancing yield stress of cement paste through in-situ polymerization and uncover the mechanisms of in-situ polymerized polymers. We investigate the effects of two types of in-situ polymerized polymer, sodium polyacrylate (PAAS) and polyacrylamide (PAM), on the yield stress, interstitial solution viscosity, and flocculated structure, as well as their adsorption behaviors on the surface of cement particles. The results show that the yield stresses of both in-situ polymerization modified cement pastes are raised considerably at high polymer concentration, which can be attributed to the dual roles of generated polymers. On the one hand, the absorbing polymers can bridge cement particles together, resulting in an augmentation in the interparticle forces. On the other hand, the non-adsorbing polymers remaining in the interstitial solution interact with each other and create a robust polymer network that can effectively withstand the external stresses. The former mechanism emerges as the dominant contributor to the enhanced yield stress of cement paste modified with in-situ polymerized PAAS, attributed to the Freundlich multilayer adsorption behavior of PAAS amplifying the bridging effect of polymers. While in-situ polymerized PAM predominantly assume the latter role, largely due to the remarkable length of their chain structure and the abundant residual polymers in the interstitial solution, which greatly intensities the interaction between polymers.

Mechanical Properties of Palygorskite Clay Stabilized with Polyelectrolytes

Two polyelectrolytes of opposite charges, sodium polystyrene sulfonate (PSS) and polydiallyldimethylammonium chloride (PDADMAC), were investigated to stabilize palygorskite clay at varying dosages of 0.2, 0.8, 1.6, and 3.2 % by the dry weight of the soil. Both PSS and PDADMAC improved the unconfined compressive strength of the palygorskite clay. PSS was effective at all the polymer contents studied after 7 days of dry curing and the strength increased with the dosages of PSS added, ranging from 2 MPa (0.2 % PSS) to 3.1 MPa (3.2 % PSS), compared with 1.5 MPa of the untreated soil. PDADMAC, on the other hand, showed comparable strength improvements as PSS did at the high polymer contents of 1.6 and 3.2 % but did not work at 0.2 and 0.8 % dosages. Under wet curing at 100 % relative humidity, PSS improved the strength of the clay by 40 % (620 kPa at 0.2 % PSS) to 77 % (764 kPa at 1.6 % PSS) compared to the untreated clay (440 kPa). PDADMAC exhibited less improvement than PSS under wet conditions but still worked at dosages of 0.8 and 1.6 %. Besides strength, the resilient modulus and fracture toughness of the treated specimens increased by approximately 10 % and 66 %, respectively, when treated with 1.6 % PSS, which was the optimum content based on the strength results. PDADMAC-treated palygorskite, however, exhibited cracking during curing for both tests, showing potential drying crack issues. The adsorption of PSS and PDADMAC on palygorskite clay were also measured using ultraviolet–visible spectroscopy, and binding between these polymers and palygorskite has been confirmed. The measured adsorption capacities of PSS and PDADMAC were comparable (2.9 and 2.7 mg/g, respectively), while the PSS was somewhat more efficient in improving soil mechanical properties.

Mixing performance of an expansive mixer on viscoelastic solutions under alternating current electric field

Development of effective technologies for mixing viscoelastic solutions with reagents is still a challenge, which plays an important role in the fields of disease diagnosis, water desalination, and immunoassay. The purpose of this paper is to numerically study the mixing performance of an expansive mixer on the viscoelastic solution under the impact of an alternating current (AC) electric field through the analyzation of mixing efficiency, the concentration distribution, and average outlet velocity. A poly acrylic acid (PAA) water solution with different concentrations characterized by the Oldroyd-B constitutive model is used as a mixed medium, and an open-source toolbox called rheoTool based on finite volume algorithm is applied to solve the governing equations. We quantitatively determine the mixing efficiency for different PAA concentrations, AC electric field strengths, and frequencies and compare the mixing efficiency created by AC and direct current (DC) electric fields. Our investigation indicates that the mixing efficiency of the mixer diminishes with the PAA concentrations but enhances with the AC electric field strengths for a relatively high polymer concentration, and AC electric fields with different frequencies lead to a larger mixing efficiency than DC electric fields for a low polymer concentration. Additionally, the influence of the model parameters on the average outlet velocity and concentration distribution is discussed at length. Our numerical simulation results show that the mixer has an excellent mixing performance for both Newtonian and viscoelastic solutions, with a mixing efficiency of more than 99% at a low polymer concentration and a stable outflow velocity.

Shear Thickening Behavior in Injectable Tetra-PEG Hydrogels Cross-Linked via Dynamic Thia-Michael Addition Bonds.

Injectable poly(ethylene glycol) (PEG)-based hydrogels were reversibly cross-linked through thia-conjugate addition bonds and demonstrated to shear thicken at low shear rates. Cross-linking bond exchange kinetics and dilute polymer concentrations were leveraged to tune hydrogel plateau moduli (from 60 to 650 Pa) and relaxation times (from 2 to 8 s). Under continuous flow shear rheometry, these properties affected the onset of shear thickening and the degree of shear thickening achieved before a flow instability occurred. The changes in viscosity were reversible whether the shear rate increased or decreased, suggesting that chain stretching drives this behavior. Given the relevance of dynamic PEG hydrogels under shear to biomedical applications, their injectability was investigated. Injection forces were found to increase with higher polymer concentrations and slower bond exchange kinetics. Altogether, these results characterize the nonlinear rheology of dilute, dynamic covalent tetra-PEG hydrogels and offer insight into the mechanism driving their shear thickening behavior.

Continuous Manufacturing of Solvent-Free Cyclodextrin Inclusion Complexes for Enhanced Drug Solubility via Hot-Melt Extrusion: A Quality by Design Approach.

Conventional cyclodextrin complexation enhances the solubility of poorly soluble drugs but is solvent-intensive and environmentally unfavorable. This study evaluated solvent-free hot-melt extrusion (HME) for forming cyclodextrin inclusion complexes to improve the solubility and dissolution of ibuprofen (IBU). Molecular docking confirmed IBU's hosting in Hydroxypropyl-β-cyclodextrin (HPβ-CD), while phase solubility revealed its complex stoichiometry and stability. In addition, an 11 mm twin-screw co-rotating extruder with PVP VA-64 as an auxiliary substance aided the complex formation and extrusion. Using QbD and the Box-Behnken design, we studied variables (barrel temperature, screw speed, and polymer concentration) and their impact on solubility and dissolution. The high polymer concentration and high screw speeds positively affected the dependent variables. However, higher temperatures had a negative effect. The lowest barrel temperature set near the Tg of the polymer, when combined with high polymer concentrations, resulted in high torques in HME and halted the extrusion process. Therefore, the temperature and polymer concentration should be selected to provide sufficient melt viscosities to aid the complex formation and extrusion process. Studies such as DSC and XRD revealed the amorphous conversion of IBU, while the inclusion complex formation was demonstrated by ATR and NMR studies. The dissolution of ternary inclusion complexes (TIC) produced from HME was found to be ≥85% released within 30 min. This finding implied the high solubility of IBU, according to the US FDA 2018 guidance for highly soluble compounds containing immediate-release solid oral dosage forms. Overall, the studies revealed the effect of various process parameters on the formation of CD inclusion complexes via HME.

Preparing cyclic polymers at high concentrations via self-folding cyclization technique by adjusting the contents of hydrophilic units in linear precursors

Cyclic polymers are a class of polymers that feature endless topology, and the synthesis of cyclic polymers has attracted the attention of many researchers. Herein, cyclic polymers were efficiently constructed by self-folding cyclization technique at high concentrations. Linear poly((oligo(ethylene glycol)acrylate)-co-(dodecyl acrylate)) (P(OEGA-co-DDA)) precursors with different ratios of hydrophilic and hydrophobic moieties were synthesized by reversible addition-fragmentation chain transfer (RAFT) polymerization using a bifunctional chain transfer agent with two anthryl end groups. The amphiphilic linear precursors underwent the self-folding process to generate polymeric nanoparticles in water. By irradiating the aqueous solution of the nanoparticles with 365 nm UV light, cyclic polymers were synthesized successfully via coupling of anthryl groups. The effects of the ratios of hydrophilic and hydrophobic moieties in linear P(OEGA-co-DDA) copolymers and polymer concentration on the purity of the obtained cyclic polymers were explored in detail via1H nuclear magnetic resonance (1H NMR), dynamic light scattering (DLS), UV‒visible (vis) analysis, three-detection size exclusion chromatography (TD-SEC) and transmission electron microscopy (TEM). It was found that by adjusting the content of the hydrophilic segments in linear precursors, single chain polymeric nanoparticles (SCPNs) can be generated at high polymer concentrations. Therefore, cyclic polymers with high purity can be constructed efficiently. This method overcomes the limitation of traditional ring-closure method, which is typically conducted in highly dilute conditions, providing an efficient method for the scalable preparation of cyclic polymers.

Influence of polymer on the surface quality and microstructure in a novel additive manufacturing method using metal paste

A new additive manufacturing method using metal paste was developed, in order to reduce waste caused by powder recycling in conventional powder bed fusion and maintain a high density in the fabricated parts. The paste was composed of metal powder, polymer particles, and a volatile solvent. Experiments were conducted to investigate the influence of a low polymer content on the paste during processing, surface topology before and after melting, and microstructure of the single-layer samples. The results showed that polymer addition could prevent the formation of powder clots by improving homogeneity of the metal paste and suppressing defect generation. The polymer also led to a smoother surface by reducing the spatter size. Finer grains were observed in the sample produced at higher polymer content.

Drug-Polymer Miscibility and the Overlap Concentration (C*) as Measured by Rheology: Variation of Polymer Structure.

Amorphous solid dispersions (ASDs), wherein a drug is molecularly dispersed in a polymer, can improve physical stability and oral bioavailability of poorly soluble drugs. Risk of drug crystallization is usually averted using high polymer concentrations. However, we demonstrated recently that the overlap concentration, C*, of polymer in drug melt is the minimum polymer concentration required to maintain drug in the amorphous state following rapid quench. This conclusion was confirmed for several drugs mixed with poly(vinylpyrrolidone) (PVP). Here we assess the solid-state stability of ASDs formulated with a variety of polymers and drugs and at various polymer concentrations (C) and molecular weights (MWs). We further test the hypothesis that degree of drug crystallization decreases with increasing C/C* and vanishes when C>C*, where C* depends on polymer MW and strength of drug-polymer interaction. We test our hypothesis with ASDs consisting of ketoconazole admixed with polyacrylic acid, polymethacrylic acid and poly (methacrylic acid-co-ethyl acrylate); and felodipine admixed with PVP and poly (vinylpyrrolidone-co-vinyl acetate). Values of C* for polymers in molten drug are rheologically determined. Crystallization behavior is assessed by measuring enthalpy of fusion, ΔHf and by X-ray diffraction. We confirm that ΔHf/ΔHf, C = 0 = f(C/C∗), and essentially no crystallization occurs when C>C*. Our findings will aid researchers in designing or selecting appropriate polymers to inhibit crystallization of poorly soluble drugs. This research also suggests that C* as determined by rheology can be used to compare drug-polymer interactions for similar molecular weight polymers.

Unraveling the Phase Behavior, Mechanical Stability, and Protein Reconstitution Properties of Polymer-Lipid Hybrid Vesicles.

Hybrid vesicles consisting of natural phospholipids and synthetic amphiphilic copolymers have shown remarkable material properties and potential for biotechnology, combining the robustness of polymers with the biocompatibility of phospholipid membranes. To predict and optimize the mixing behavior of lipids and copolymers, as well as understand the interaction between the hybrid membrane and macromolecules like membrane proteins, a comprehensive understanding at the molecular level is essential. This can be achieved by a combination of molecular dynamics simulations and experiments. Here, simulations of POPC and PBD22-b-PEO14 hybrid membranes are shown, uncovering different copolymer configurations depending on the polymer-to-lipid ratio. High polymer concentrations created thicker membranes with an extended polymer conformation, while high lipid content led to the collapse of the polymer chain. High concentrations of polymer were further correlated with a decreased area compression modulus and altered lateral pressure profiles, hypothesized to result in the experimentally observed improvement in membrane protein reconstitution and resistance toward destabilization by detergents. Finally, simulations of a WALP peptide embedded in the bilayer showed that only membranes with up to 50% polymer content favored a transmembrane configuration. These simulations correlate with previous and new experimental results and provide a deeper understanding of the properties of lipid-copolymer hybrid membranes.

Molecular Processes Leading to Shear Banding in Entangled Polymeric Solutions.

The temporal and spatial evolution of shear banding during startup and steady-state shear flow was studied for solutions of entangled, linear, monodisperse polyethylene C3000H6002 dissolved in hexadecane and benzene solvents. A high-fidelity coarse-grained dissipative particle dynamics method was developed and evaluated based on previous NEMD simulations of similar solutions. The polymeric contribution to shear stress exhibited a monotonically increasing flow curve with a broad stress plateau at intermediate shear rates. For startup shear flow, transient shear banding was observed at applied shear rates within the steady-state shear stress plateau. Shear bands were generated at strain values where the first normal stress difference exhibited a maximum, with lifetimes persisting for up to several hundred strain units. During the lifetime of the shear bands, an inhomogeneous concentration distribution was evident within the system, with higher polymer concentration in the slow bands at low effective shear rate; i.e., γ˙<τR-1, and vice versa at high shear rate. At low values of applied shear rate, a reverse flow phenomenon was observed in the hexadecane solution, which resulted from elastic recoil of the molecules within the slow band. In all cases, the shear bands dissipated at high strains and the system attained steady-state behavior, with a uniform, linear velocity profile across the simulation cell and a homogeneous concentration.

Biomimetic Spun Silk Ionotronic Fibers for Intelligent Discrimination of Motions and Tactile Stimuli.

Innovation in the ionotronics field has significantly accelerated the development of ultraflexible devices and machines. However, it is still challenging to develop efficient ionotronic-based fibers with necessary stretchability, resilience, and conductivity due to inherent conflict in producing spinning dopes with both high polymer and ion concentrations and low viscosities. Inspired by the liquid crystalline spinning of animal silk, this study circumvents the inherent tradeoff in other spinning methods by dry spinning a nematic silk microfibril dope solution. The liquid crystalline texture allows the spinning dope to flow through the spinneret and form free-standing fibers under minimal external forces. The resultant silk-sourced ionotronic fibers (SSIFs) are highly stretchable, tough, resilient, and fatigue-resistant. These mechanical advantages ensure a rapid and recoverable electromechanical response of SSIFs to kinematic deformations. Further, the incorporation of SSIFs into core-shell triboelectric nanogenerator fibers provides outstanding stable and sensitive triboelectric response to precisely and sensitively perceive small pressures. Moreover, by implementing a combination of machine learning and Internet of Things techniques, the SSIFs can sort objects made of different materials. With these structural, processing, performance, and functional merits, the SSIFs prepared herein are expected to be applied in human-machine interfaces.

Extensional rheometry of mobile fluids. Part II: Comparison between the uniaxial, planar, and biaxial extensional rheology of dilute polymer solutions using numerically optimized stagnation point microfluidic devices

Part I of this paper [Haward et al., J. Rheol. 67, 995–1009 (2023)] presents a three-dimensional microfluidic device (the optimized uniaxial and biaxial extensional rheometer, OUBER) for generating near-homogeneous uniaxial and biaxial elongational flows. Here, in Part II, the OUBER device is employed to examine the uniaxial and biaxial extensional rheology of model dilute polymer solutions, compared with measurements made under planar extension in the optimized-shape cross-slot extensional rheometer [OSCER, Haward et al. Phys. Rev. Lett. 109, 128301 (2012)]. In each case, micro-particle image velocimetry is used to measure the extension rate as a function of the imposed flow conditions, and excess pressure drop measurements enable estimation of the tensile stress difference generated in the fluid via a new analysis based on the macroscopic power balance for flow through each device. Based on this analysis, for the most dilute polymer sample tested, which is “ultradilute”, the extensional viscosity is well described by Peterlin’s finitely extensible nonlinear elastic dumbbell model. In this limit, the biaxial extensional viscosity at high Weissenberg numbers (Wi) is half that of the uniaxial and planar extensional viscosities. At higher polymer concentrations, although the fluids remain dilute, the experimental measurements deviate from the model predictions, which is attributed to the onset of intermolecular interactions as the polymer chains unravel in the extensional flows. Of practical significance (and fundamental interest), elastic instability occurs at a significantly lower Wi in uniaxial extensional flow than in either biaxial or planar extensional flow, thereby limiting the utility of this flow type for extensional viscosity measurement.