Polymer Coils Research Articles

Using the Herschel-Bulkley Consistency Index to Characterise Complex Biopolymer Systems-The Effect of Screening.

The use of the consistency index, as determined from fitting rheological data to the Herschel-Bulkley model, is described such that it may yield systematic trends that allow a very convenient description of the dissipative flow properties of linear and branched (bio)polymers in general, both in molecular and weakly associated supramolecular solutions. The effects of charge-mediated interactions by the systematic variation of the ionic strength and hydrogen bonding by a systematic variation in pH, using levels that are frequently encountered in systems used in practice, is investigated. These effects are then captured using the associated changes in the intrinsic viscosity to highlight the above-mentioned trends, while it also acts as an internal standard to describe the data in a concise form. The trends are successfully captured up to 100 times the polymer coil overlap and 100,000 times the solvent viscosity (or consistency index). These results therefore enable the rapid characterization of biopolymer systems of which the morphology remains unknown and may continue to remain unknown due to the wide-ranging monomer diversity and a lack of regularity in the structure, while the macromolecular coil size may be determined readily.

An Exceptionally Salt Tolerant Copoly(Maleimide Sulfobetaine) - Structural Requirements for Ultra-Salt Tolerance.

Zwitterionic polymers are an important class of polymers with far-ranging applications. In the widely studied poly(meth)acrylate and poly(meth) acrylamide-based zwitterions, properties can be tuned by changing the nature of substituents attached to ammonium ions. However, these changes influenced salt tolerance of zwitterionic polymers only to a limited extent. Upon adding salt these polymers expanded in solution initially. Further increase in salt concentration caused the polymer chains to shrink similar to the common water soluble, uncharged polymers thereby deteriorating the viscosity of aqueous solutions. In contrast to the conventional poly(meth)acrylate and poly(meth)acrylamide-based zwitterions, zwitterionic copolymaleimides showed substituent dependent salt-tolerant nature. In the absence of any substituent on the polymer backbone such as zwitterionic poly(ethylene-alt-maleimide) (ZI-PEMA) the viscosity of salt solutions increased both with the increasing salt concentration as well as the concentration of polymer. This is likely due to the continuous expansion of polymer coil in salt solutions with increasing salt concentration caused primarily by the rigidity of the polymer backbone. ZI-PEMA also enhanced the saturation limit of mono- and divalent salts like sodium chloride and hydrated calcium bromide in water. This property is useful for various applications like fish curing, for making high-density fluids, refrigeration, etc. across various industrial sectors.

Compound Model of Twisted and Coiled Polymer Actuators Describing Relationship Between Output Force and Excitation Current

Compound Model of Twisted and Coiled Polymer Actuators Describing Relationship Between Output Force and Excitation Current

Coil Formation and Biomimetic Performance Characterization of Twisted Coiled Polymer Artificial Muscles

A biological muscle's force is nonlinearly constrained by its current state (force, length, and speed) and state history. To investigate if artificial muscles can mimic (i.e. biomimetic) the complete mechanical state spectrum of biological muscles, this study uses a novel method to characterize twisted coiled polymer actuators (TCPAs) mechanically. Thus, comprehensive and reproducible test procedures are established to verify artificial muscle biomimetics regarding stress, strain, and strain rate combinations intrinsic to biological muscle. A rheometer performs novel high‐precision mechanical characterization methods to comprehensively verify biomimetic performance. Sample twist level, torque, length, force, and temperature are controlled and measured during twist‐induced coiling, heatsetting/annealing, and mechanical testing. TCPAs are formed from linear low‐density polyethylene monofilament. Linear low‐density polyethylene (LLDPE) TCPAs generate larger stresses than biological muscle through the entire spectrum of strains—contracting more than 40%, exerting more than 0.3 MPa at rest length, and withstanding tension of 8 MPa without damage. Thus, the LLDPE TCPAs attain biological muscle performance statically, but additional tests are required to assess this dynamically. The mechanical performance of LLDPE TCPAs enables biomimetic actuation with an intelligent control and measurement system. Their high‐throughput textile manufacturability positions them for advanced biomechatronic applications—including prosthetics and exoskeletons.

Monte Carlo simulation for the effect of chain stiffness on the free surface of polymer melts

The role of chain stiffness on structural and molecular properties for the free surface of polymer melts was examined by Monte Carlo (MC) simulations of the coarse-grained (CG) polyethylene-like chains on the second nearest neighbor diamond (2nnd) lattice. Polyethylene-like model by multiplying the statistical weights with the chain stiffness parameter (k) to represent more flexible (k = 0.0 and 0.5) and stiffer (k = 1.5 and k = 2.0) chains than normal polyethylene (k = 1.0). For the melt-vacuum surfaces of stiffer chains, bulk densities become lower with broader surface profiles. For more flexible chains, monomers at the end/middle position are more segregated/depleted near the surface. Bonds and chains tend to be randomly orientated in the bulk region but exhibit anisotropic orientation near the surface, especially for stiffer chains. For more flexible chains, polymers adopt a larger amount of gauche conformation and chain dimensions become smaller with a more compact shape. The main principal axes of polymer coils are preferably oriented parallelly to the surface and the magnitudes of this anisotropy are larger for stiffer chains. Based on intra- and intermolecular energetics, more flexible chains have a larger amount of gauche conformation with denser bulk structures but they adopt more trans conformation near the surface.

A Numerical Model of Heating and Cooling Cycles to Study the Driven Response for Twisted and Coiled Polymer Actuator

A Numerical Model of Heating and Cooling Cycles to Study the Driven Response for Twisted and Coiled Polymer Actuator

Poly(butylene terephthalate) Copolyesters with Dilinoleic Derivatives: Solution Properties and Influence of Short‐Chain Branching

AbstractThe solution behavior of poly(butylene terephthalate) (PBT) copolyesters with dilinoleic monomer units (dilinoleic diol (LD) / dilinoleic diacid (LA)) is studied to understand the processing behavior from melt. NMR investigations show that the short‐chain branches are characterized by a distribution of different alkyl chain lengths, where n‐butyl (C4) and longer chains have the largest content (>55 mol%). High‐temperature size exclusion chromatography with threefold detection (multi‐angle light‐scattering, refractive index, and viscosity detector) in 1,2,4‐trichlorobenzene is performed to determine molar masses, hydrodynamic radii, viscosity radii, and Kuhn–Mark–Houwink–Sakurada (KMHS) exponents α in dependence of the molar amount of short‐chain branched comonomers. Low concentrations of dilinoleic comonomers in PBT copolyesters improve the solubility of the copolyesters significantly. Higher amounts cause contraction of the polymer coils as illustrated by smaller hydrodynamic radii as well as lower KMHS exponents. The α values decrease with increasing amount of short‐chain branched comonomer except for very low concentrations. The solution behavior of LA and LD copolyesters with a higher aliphatic content shows different trends of the influence of short‐chain branches on the melt behavior, which reflects the influence of intramolecular versus intermolecular entanglements in solution and in melt.

Pressure-assisted vacuum filtration fabrication of polymer membranes with enhanced selectivity for the separation of an ethanol/carbon dioxide mixture

The membrane performance and effectiveness of fabrication are significant factors that determine the industrialization of membranes. In this study, a pressure-assisted vacuum filtration method was proposed to fabricate a sub-100 nm thin composite membrane using a homemade polyamide for the separation of an ethanol/carbon dioxide (CO2) mixture. Because during bioethanol fermentation, a large amount of CO2 can be produced, forming fermentation tail gas with vaporized ethanol, which should be separated to recover ethanol and reduce greenhouse CO2 emissions. The fabrication conditions, including the size of the polymer coil and feed pressure, were investigated in detail. Characterization using a dynamic laser scatterometer and low-field nuclear magnetic resonance (NMR) was conducted to reveal the membrane properties. The membrane performance obtained by the pressure-assisted vacuum filtration method was compared with that obtained by the solution casting method, which was demonstrated to be 40 % higher. Meanwhile, when a smaller pore size of the substrate was used, a 56 nm thick composite membrane was obtained with an ethanol/CO2 selectivity of 18 and an ethanol permeance of approximately 35000 GPU (1960 Barrer). Finally, the effects of the operating parameters, such as the feed concentration and stability, on the membrane performance were investigated. This study provides a valuable reference for the fabrication of ultrathin polymer membranes.

Wetting of alginate aerogels, from mesoporous solids to hydrogels: a small-angle scattering analysis

Mesoporous polysaccharide aerogels are versatile functional materials for drug delivery and wound dressing devices. The hydration and wetting of these aerogels control their application-related performance, e.g. the release of encapsulated drugs. Reported here is a detailed small-angle neutron scattering (SANS) analysis of the hydration mechanism of a calcium alginate aerogel, based on mathematical modelling of the scattering. The model accounts for the hierarchical structure of the material comprising a mesoporous structure, the solid skeleton of which is made up of water-swollen polymers. At large scale, the mesoporous structure is modelled as a random collection of elongated cylinders, which grow in size as they absorb water and aggregate. The small-scale inner structure of the skeleton is described as a Boolean model of polymer coils, which captures the progressive transition from a dense dry polymer to a fully hydrated gel. Using known physico-chemical characteristics of the alginate, the SANS data are fitted using the size of the cylinders as the only adjustable parameter. The alginate aerogel maintains a nanometre-scale, albeit altered, structure for low water contents but it collapses into micrometre-sized structures when the water content approaches one gram of water per gram of alginate. In addition to the wetting of aerogels, the model might be useful for the small-angle scattering analysis of the supercritical drying of gels.

Crystallization Inhibition in Molecular Liquids by Polymers above the Overlap Concentration (c*): Delay of the First Nucleation Event

Low concentration polymer additives can significantly alter crystal growth kinetics of molecular liquids and glasses. However, the effect of polymer concentration on nucleation kinetics remains poorly understood. Based on an experimentally determined first nucleation time (time to form the first critical nucleus, t0), we show that the polymer overlap concentration, c*, where polymer coils in the molecular liquid start to overlap with each other, is a critical polymer concentration for efficient inhibition of crystallization of a molecular liquid. The value of t0 is approximately equal to that of the neat molecular liquid when the polymer concentration, c, is below c*, but increases significantly when c > c*. This finding is relevant for effective polymer screening and performance prediction of engineered multicomponent amorphous materials, particularly pharmaceutical amorphous solid dispersions.

Transient slow motion of a porous sphere

The start-up creeping motion of a porous spherical particle, which models a permeable polymer coil or floc of nanoparticles, in an incompressible Newtonian fluid generated by the sudden application of a body force is investigated for the first time. The transient Stokes and Brinkman equations governing the fluid velocities outside and inside the porous sphere, respectively, are solved by using the Laplace transform. An analytical formula for the transient velocity of the particle as a function of relevant parameters is obtained. As expected, the particle velocity increases over time, and a particle with greater mass density lags behind a corresponding less dense particle in the growth of the particle velocity. In general, the transient velocity is an increasing function of the porosity of the particle. On the other hand, a porous particle with a higher fluid permeability will have a greater transient velocity than the same particle with a lower permeability, but may trail behind the less permeable particle in the percentage growth of the velocity. The acceleration of the porous particle is a monotonic decreasing function of the elapsed time and a monotonic increasing function of its fluid permeability. In particular, the transient behavior of creeping motions of porous particles may be much more important than that of impermeable particles.

Effective On-Line Performance Modulation and Efficient Continuous Preparation of Ultra-Long Twisted and Coiled Polymer Artificial Muscles for Engineering Applications.

Artificial muscle is a kind of thread-like actuator that can produce contractile strain, generate force, and output mechanical work under external stimulations to imitate the functions and achieve the performances of biological muscles. It can be used to actuate various bionic soft robots and has broad application prospects. The electrically controlled twisted and coiled polymer (TCP) artificial muscles, with the advantages of high power density, large stroke and low driving voltage, while also being electrolyte free, are the most practical. However, the relationship between the muscle performances and its preparation parameters is not very clear yet, and the complete procedure of designing and preparing TCP muscles according to actual needs has not been established. Besides, current preparation approaches are very time-consuming and cannot make ultra-long TCP muscles. These problems greatly limit wide applications of TCP artificial muscles. In this study, we studied and built the relationship between the actuating performances of TCP muscles and their preparation parameters, so that suitable TCP muscles can be easily designed and prepared according to actual requirements. Moreover, an efficient preparation method integrating one-step annealing technique has been developed to realize on-line performance modulation and continuous fabrication of ultra-long TCP muscles. By graphically assembling long muscles on heat-resist films, we designed and produced a series of fancy soft robots (butterfly, flower, starfish), which can perform various bionic movements and complete specific tasks. This work has achieved efficient on-demand preparation and large-scale assembly of ultra-long TCP muscles, laying solid foundations for their engineering applications in soft robot field.

ХАРАКТЕРИСТИЧЕСКАЯ ВЯЗКОСТЬ РАСТВОРА ПОЛИМЕРА

A fractal model of the structure of polymer macromolecules in solution is used to derive an analogue of Mark-Kuhn-Houwink-Sakurada empirical equation linking the intrinsic viscosity of the solution with the molecular mass of the polymer. It is shown that in addition to the molecular mass, the theoretically obtained equation – on the basis of the intrinsic viscosity – makes it possible to determine the size of Kuhn's rigid segment of the polymer and the fractal dimension of the polymer coils that characterize the structure of macromolecules in solution

Effects of Manufacturing Parameters on Fast Actuation of Twisted and Coiled Polymer Actuators Made of Fishing Lines

Effects of Manufacturing Parameters on Fast Actuation of Twisted and Coiled Polymer Actuators Made of Fishing Lines

Preparation of Preformed Submicron Crosslinked Polymer Coils for Conformance Control in Low-Permeability Reservoirs.

With the increasing development of low-permeability reservoirs, the significance of conformance control treatment has risen considerably. To address the conflict between injectability and plugging performance, as well as to enhance the deep migration capacity of conformance control agents, preformed submicron crosslinked polymer coils (SCPCs) have been manufactured using aqueous solution dispersion polymerization. Fourier transform infrared and scanning electron microscopy were employed to examine the chemical structure and micromorphology, while particle size distribution, zeta potential, rheological, and filtration properties were analyzed. The effectiveness of conformance control was confirmed through the parallel core displacement. The effective particle size of SCPCs was at a submicron level (500~800 nm). SCPCs exhibit a transitional threshold concentration between gel and sol states (0.25 wt%~0.5 wt%). SCPCs can efficiently block the 1.2 μm microporous filter membrane. The filtration time is up to 67.8 min. SCPCs can improve the water absorption rate of lower permeability cores from 21.21% to 57.89% with a permeability difference of 5. Therefore, SCPCs have good injectability, plugging performance, and deep migration capacity and can be used for conformance control in low-permeability reservoirs.

A comparative study of polymer viscosity modifiers: Flow field challenges & alternative trends

In recent years, substantial advancements have been achieved in augmenting the energy efficiency of hydraulic fluids through the integration of polymers. This study employs a multiscale approach, encompassing an analysis of polymer coil size evolution and flow field characteristics, with the aim of investigating the behavior of both dipole and non-dipole polymers within the host solvent. The ultimate goal is to establish a comprehensive understanding of the correlation between atomic properties of additives and the macroscopic properties of the polymer solution.To achieve this, the study employs an atomistic-continuum hybrid model that combines Brownian Dynamics and Lattice Boltzmann techniques within the bead-spring concept framework. Four chains, each comprising 64 particles, are subjected to varying shear rates. The primary focus centers on the examination of alterations in the radius of gyration and the velocity field within the polymer solution. Notably, the inclusion of dipole-dipole interactions exerts a profound influence on the configuration of the polymers. The results illuminate that non-dipole polymers display a more pronounced coupling with bulk flow hydrodynamics, leading to the confinement of particle motion in directions perpendicular to the primary stream. In contrast, dipole polymers experience a slower increase in coil size when compared to their non-dipole counterparts. These findings furnish valuable insights for the enhancement of energy-efficient hydraulic fluids and contribute to a fundamental comprehension of polymer behavior in lubricants, charting the course for the development of advanced hydraulic fluids in the future.

Density Fluctuations Inside an Individual Polymer Coil.

More than five hundred images of individual macromolecules of random styrene-butadiene copolymers and styrene-isoprene block copolymers dissolved in a polystyrene matrix were analyzed. The presence of density fluctuations inside the macromolecular coil has been established. Within the framework of the model of harmonic oscillations, the radial distribution of such density fluctuations is estimated.

Hydraulic conductivity and multi-scale pore structure of polymer-enhanced geosynthetic clay liners permeated with bauxite liquors

A study was conducted to investigate the multi-scale pore structure-based mechanism controlling the hydraulic conductivity of polymer-enhanced geosynthetic clay liners (GCLs) prepared by the wet-mixed method to bauxite liquors (BLS and BLA). The multi-scale pore structures were evaluated using MIP and N2GA tests quantitatively. Conventional GCL permeated with BLS had a larger flow path volume than with DI water (0.194 > 0.119 cm³/g), attributed to the bentonite swelling inhibition and the montmorillonite dissolution, leading to the higher hydraulic conductivity (3.0 × 10−7 > 2.7 × 10−11 m/s). Polymer-enhanced GCLs developed more micropores and had a smaller quantity proportion and volume of flow paths since polymer formed more micropores to clog pores, contributing to a lower hydraulic conductivity than conventional GCL to BLS. The hydraulic conductivity of polymer-enhanced GCL to BLS (ionic strength: 622.5 mM) was higher than that to BLA (156.9 mM) (2.6 × 10−9 > 6.0 × 10−12 m/s), given that the coiled or contracted polymer conformation left a smaller quantity proportion (5.54% < 6.71%) and volume (0.0002 cm3/g < 0.0035 cm3/g) of micropores.

Evaluation of a novel polymer coil for endovascular occlusion of intracranial aneurysms in a rabbit model.

The results of the preclinical study of a novel polymer coil in treatment of elastase induced aneurysms will be presented in this paper. We induced 16 aneurysms in 16 New Zealand white rabbits at the origin of the right common carotid artery at the brachiocephalic trunk. Newly developed polymer coils in both groups for six aneurysms each and platinum coils for two aneurysms each were used. Control angiographies followed in both groups immediately after coiling as well as in the first eight animals 30days after intervention (30days group) and in the other eight animals 90days after (90days group). An explanation and histological evaluation of the treated aneurysms followed. The 12 animals in which the aneurysms were treated with polymer coils showed a complete occlusion (grade IV) in only 6 out of 12 aneurysms (50%), an almost complete occlusion (grade III) in 5 out of 12 (42%) and an incomplete occlusion in the treatment of one aneurysm (8%). Histologically, we observed a significantly more pronounced inflammatory response and neoangiogenesis in aneurysms treated with polymer coils only in the 30days group. Most difficulties and concerns with the polymer coils were related to the flexibility and detachment behaviour. Therefore, and due to the technical challenges of delivery, the novel polymer coil cannot be considered an alternative to the current platinum coils.

HBS-1.2: Lightweight Socially Assistive Robot with 6-Ply Twisted Coiled Polymer Muscle-Actuated Hand

In this paper, a new socially assistive robot (SARs) called HBS-1.2 is presented, which uses 6-ply twisted and coiled polymer (TCP) artificial muscles in its hand to perform physical tasks. The utilization of 6-ply TCP artificial muscles in a humanoid robot hand is a pioneering advancement, offering cost effective, lightweight, and compact solution for SARs. The robot is designed to provide safer human–robot interaction (HRI) while performing physical tasks. The paper explains the procedures for fabrication and testing of the 6-ply TCP artificial muscles, along with improving the actuation response by using a Proportional-Integral-Derivative (PID) control method. Notably, the robot successfully performed a vision-based pick and place experiment, showing its potential for use in homecare and other settings to assist patients who suffer from neurological diseases like Alzheimer’s disease. The study also found an optimal light intensity range between 34 to 108 lumens/m2, which ensures minimal variation in calculated distance with 95% confidence intervals for robust performance from the vison system. The findings of this study have important implications for the development of affordable and accessible robotic systems to support elderly patients with dementia, and future research should focus on further improving the use of TCP actuators in robotics.