Browse
Submit Data
Databases
API
Help

Dataset Information

32 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Ultrahigh energy-dissipation elastomers by precisely tailoring the relaxation of confined polymer fluids.

ABSTRACT: Energy-dissipation elastomers relying on their viscoelastic behavior of chain segments in the glass transition region can effectively suppress vibrations and noises in various fields, yet the operating frequency of those elastomers is difficult to control precisely and its range is narrow. Here, we report a synergistic strategy for constructing polymer-fluid-gels that provide controllable ultrahigh energy dissipation over a broad frequency range, which is difficult by traditional means. This is realized by precisely tailoring the relaxation of confined polymer fluids in the elastic networks. The symbiosis of this combination involves: elastic networks forming an elastic matrix that displays reversible deformation and polymer fluids reptating back and forth to dissipate mechanical energy. Using prototypical poly (n-butyl acrylate) elastomers, we demonstrate that the polymer-fluid-gels exhibit a controllable ultrahigh energy-dissipation property (loss factor larger than 0.5) with a broad frequency range (10^-2 ~ 10⁸ Hz). Energy absorption of the polymer-fluid-gels is over 200 times higher than that of commercial damping materials under the same dynamic stress. Moreover, their modulus is quasi-stable in the operating frequency range.

SUBMITTER: Huang J

PROVIDER: S-EPMC8203694 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Precisely Tailoring Upconversion Dynamics via Energy Migration in Core-Shell Nanostructures.

Project description:Upconversion emission dynamics have long been believed to be determined by the activator and its interaction with neighboring sensitizers. Herein this assumption is, however, shown to be invalid for nanostructures. We demonstrate that excitation energy migration greatly affects upconversion emission dynamics. "Dopant ions' spatial separation" nanostructures are designed as model systems and the intimate link between the random nature of energy migration and upconversion emission time behavior is unraveled by theoretical modelling and confirmed spectroscopically. Based on this new fundamental insight, we have successfully realized fine control of upconversion emission time behavior (either rise or decay process) by tuning the energy migration paths in various specifically designed nanostructures. This result is significant for applications of this type of materials in super resolution spectroscopy, high-density data storage, anti-counterfeiting, and biological imaging.

| S-EPMC5887923 | biostudies-literature

Bioinspired Engineering towards Tailoring Advanced Lignin/Rubber Elastomers.

Project description:The pursuit of high volume and high value-added applications for lignin has been a long-term challenge. In this work, inspired by the energy sacrificial mechanism from biological materials, we developed high-performance lignin/carbon black (CB)/nitrile rubber (NBR) elastomers by constructing a dual-crosslinking network consisting of sulfur covalent bonds and dynamic coordination sacrificial bonds. Lignin was not only used for the substitution of half mass of CB in the NBR elastomer but also served as natural ligands for the Zn-based coordination bonds, providing a significant synergistic coordination enhancement effect. The mechanical performance of the elastomers can be easily manipulated by adjusting the proportion of non-permanent coordination bonds and permanent covalent bonds. Lignin/CB/NBR elastomers with a higher strength and modulus than CB-filled elastomers were obtained while maintaining excellent elasticity. The thermal stability and the high-temperature oil resistance of NBR elastomers were also improved by incorporation of lignin and metal coordination bonds. Overall, this work inspires a new solution for the design of high-performance lignin/rubber elastomers with a high lignin loading content.

| S-EPMC6403759 | biostudies-literature

Soft elasticity optimises dissipation in 3D-printed liquid crystal elastomers.

Project description:Soft-elasticity in monodomain liquid crystal elastomers (LCEs) is promising for impact-absorbing applications where strain energy is ideally absorbed at constant stress. Conventionally, compressive and impact studies on LCEs have not been performed given the notorious difficulty synthesizing sufficiently large monodomain devices. Here, we use direct-ink writing 3D printing to fabricate bulk (>cm3) monodomain LCE devices and study their compressive soft-elasticity over 8 decades of strain rate. At quasi-static rates, the monodomain soft-elastic LCE dissipated 45% of strain energy while comparator materials dissipated less than 20%. At strain rates up to 3000 s-1, our soft-elastic monodomain LCE consistently performed closest to an ideal-impact absorber. Drop testing reveals soft-elasticity as a likely mechanism for effectively reducing the severity of impacts - with soft elastic LCEs offering a Gadd Severity Index 40% lower than a comparable isotropic elastomer. Lastly, we demonstrate tailoring deformation and buckling behavior in monodomain LCEs via the printed director orientation.

| S-EPMC8602646 | biostudies-literature

Polymer-dispersed liquid crystal elastomers.

Project description:The need for mechanical manipulation during the curing of conventional liquid crystal elastomers diminishes their applicability in the field of shape-programmable soft materials and future applications in additive manufacturing. Here we report on polymer-dispersed liquid crystal elastomers, novel composite materials that eliminate this difficulty. Their thermal shape memory anisotropy is imprinted by curing in external magnetic field, providing for conventional moulding of macroscopically sized soft, thermomechanically active elastic objects of general shapes. The binary soft-soft composition of isotropic elastomer matrix, filled with freeze-fracture-fabricated, oriented liquid crystal elastomer microparticles as colloidal inclusions, allows for fine-tuning of thermal morphing behaviour. This is accomplished by adjusting the concentration, spatial distribution and orientation of microparticles or using blends of microparticles with different thermomechanical characteristics. We demonstrate that any Gaussian thermomechanical deformation mode (bend, cup, saddle, left and right twist) of a planar sample, as well as beat-like actuation, is attainable with bilayer microparticle configurations.

| S-EPMC5059788 | biostudies-literature

Frenkel line crossover of confined supercritical fluids.

Project description:We investigate the temperature evolution of dynamics and structure of partially confined Lennard Jones (LJ) fluids in supercritical phase along an isobaric line in the P-T phase diagram using molecular dynamics simulations. We compare the Frenkel line (FL) crossover features of partially confined LJ fluids to that of the bulk LJ fluids in supercritical phase. Five different spacings have been chosen in this study and the FL crossover characteristics have been monitored for each of these spacings for temperatures ranging from 240 K to 1500 K keeping the pressure fixed at 5000 bar. We characterize the FL crossover using density of states (DoS) function and find that partially confined supercritical fluids (SCF) exhibit a progressive shift of FL crossover point to higher temperatures for smaller spacings. While the DoS perpendicular to the walls shows persistent oscillatory modes, the parallel component exhibits a smooth crossover from an oscillatory to non-oscillatory characteristics representative of FL crossover. We find that the vanishing of peaks in DoS parallel to the walls indicates that the SCF no longer supports shear mode excitations and could serve as an identifier of the FL crossover for confined systems just as is done for the bulk. Layer heights of density profiles, self-diffusivity and the peak heights of radial distribution function parallel to the walls also feature the FL crossover consistent with the DoS criteria. Surprisingly, self-diffusivity undergoes an Arrhenius to super-Arrhenius crossover at low temperatures for smaller spacings as a result of enhanced structural order evidenced via pair-excess entropy. This feature, typical of glass-forming liquids and binary supercooled liquids, is found to develop from the glass-like characteristic slowdown and strong caging in confined supercritical fluid, evidenced via mean squared displacement and velocity autocorrelation function respectively, over intermediate timescales.

| S-EPMC6795815 | biostudies-literature

An alternating multilayer architecture boosts ultrahigh energy density and high discharge efficiency in polymer composites.

Project description:Poly(vinylidene fluoride) (PVDF)-based polymers with excellent flexibility and relatively high permittivity are desirable compared to the traditional bulk ceramic in dielectric material applications. However, the low discharge efficiency (<70%) caused by the severe intrinsic dielectric loss of these polymers result in a decrease in their breakdown strength and other problems, which limit their widespread applications. To address these outstanding issues, herein, we used a stacking method to combine poly(methyl methacrylate) (PMMA) with poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) for the synthesis of a series of alternating multilayer films with different layers. Benefitting from the blocking effect of the multilayer structure and excellent insulation performance of PMMA, simultaneous improvements in the breakdown strength and discharge efficiency of the multilayer films were achieved. Compared with the pure polymer films and other multilayer films with different layers, the film with a 9-layer structure exhibited the highest energy storage density of 25.3 J cm-3 and extremely high discharge efficiency of 84% at 728 MV m-1. Moreover, the charge and discharge performance of the other multilayer films were also better than that of P(VDF-HFP). In addition, it was also found that for the multilayer composite films with the same components, the blocking effect was reinforced with an increase in the number of layers, which led to a significant improvement in the breakdown strength. We consider that the multilayer structure can correlate with the dielectric properties of different polymer materials to enhance the energy storage of composite materials, and will provide a promising route to design high dielectric performance devices.

| S-EPMC9049627 | biostudies-literature

Internal constraints and arrested relaxation in main-chain nematic elastomers.

Project description:Nematic liquid crystal elastomers (N-LCE) exhibit intriguing mechanical properties, such as reversible actuation and soft elasticity, which manifests as a wide plateau of low nearly-constant stress upon stretching. N-LCE also have a characteristically slow stress relaxation, which sometimes prevents their shape recovery. To understand how the inherent nematic order retards and arrests the equilibration, here we examine hysteretic stress-strain characteristics in a series of specifically designed main-chain N-LCE, investigating both macroscopic mechanical properties and the microscopic nematic director distribution under applied strains. The hysteretic features are attributed to the dynamics of thermodynamically unfavoured hairpins, the sharp folds on anisotropic polymer strands, the creation and transition of which are restricted by the nematic order. These findings provide a new avenue for tuning the hysteretic nature of N-LCE at both macro- and microscopic levels via different designs of polymer networks, toward materials with highly nonlinear mechanical properties and shape-memory applications.

| S-EPMC7862651 | biostudies-literature

Engineering confined fluids to autonomously assemble hierarchical 3D structures.

Project description:The inherent coupling of chemical and mechanical behavior in fluid-filled microchambers enables the fluid to autonomously perform work, which in turn can direct the self-organization of objects immersed in the solution. Using theory and simulations, we show that the combination of diffusioosmotic and buoyancy mechanisms produce independently controlled, respective fluid flows: one generated by confining surfaces and the other in the bulk of the solution. With both flows present, the fluid can autonomously join 2D, disconnected pieces to a chemically active, "sticky" base and then fold the resulting layer into regular 3D shapes (e.g. pyramids, tetrahedrons, and cubes). Here, the fluid itself performs the work of construction and thus, this process does not require extensive external machinery. If several sticky bases are localized on the bottom surface, the process can be parallelized, with the fluid simultaneously forming multiple structures of the same or different geometries. Hence, this approach can facilitate the relatively low-cost, mass production of 3D micron to millimeter-sized structures. Formed in an aqueous solution, the assembled structures could be compatible with biological environments, and thus, potentially useful in medical and biochemical applications.

| S-EPMC10367439 | biostudies-literature

Adrenergic-induced ERK3 pathway drives lipolysis and suppresses energy dissipation

Project description:Beta-adrenergic stimulation stabilizes ERK3, resulting in the formation of a complex with MK5 and thereby driving lipolysis. A downstream target of the complex is FOXO1, which controls expression of the lipolytic enzyme ATGL. Deletion of ERK3 in mouse adipocytes inhibits lipolysis, but elevates energy dissipation.

2021-01-01 | GSE142424 | GEO

Tailoring Dense, Orientation-Tunable, and Interleavedly Structured Carbon-Based Heat Dissipation Plates.

Project description:The controllability of the microstructure of a compressed hierarchical building block is essential for optimizing a variety of performance parameters, such as thermal management. However, owing to the strong orientation effect during compression molding, optimizing the alignment of materials perpendicular to the direction of pressure is challenging. Herein, to illustrate the effect of the ordered microstructure on heat dissipation, thermally conductive carbon-based materials are fabricated by tailoring dense, orientation-tunable, and interleaved structures. Vertically aligned carbon nanotube arrays (VACNTs) interconnected with graphene films (GF) are prepared as a 3D core-ordered material to fabricate compressed building blocks of O-VA-GF and S-VA-GF. Leveraging the densified interleaved structure offered by VACNTs, the hierarchical O-VA-GF achieves excellent through-plane (41.7 W m-1 K-1 ) and in-plane (397.9 W m-1 K-1 ) thermal conductivities, outperforming similar composites of S-VA-GF (through-plane: 10.3 W m-1 K-1 and in-plane: 240.9 W m-1 K-1 ) with horizontally collapsed carbon nanotubes. As heat dissipation plates, these orderly assembled composites yield a 144% and 44% enhancement in the cooling coefficient compared with conventional Si3 N4 for cooling high-power light-emitting diode chips.

| S-EPMC9982569 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data