Existence of Bound-Rubber in Magnetorheological Elastomers and Its In°uence on Material Properties

In efforts to develop a new fabrication method for improvement of the MREs' performance, the bound-rubber phenomenon was observed in MREs. Further experiments indicate the existance of bound-rubber and it in°uences the MRE performance as well as the particle size. Both theoretical analysis and experimental results indicated that MRE performance can be improved by enhancing the ratio of particle radius to bound-rubber thickness.     

基于多链模型的磁流变弹性体剪切模量的数值分析

Based on the magnetic interaction energy, using derivative of the magnetic energy density, a model is proposed to compute the magnetic-induced shear modulus of magnetorheological elastomers. Taking into account the influences of particles in the same chain and the particles in all adjacent chains, the traditional magnetic dipole model of the magnetorheological elastomers is modified. The influence of the ratio of the distance etween adjacent chains to the distance between adjacent particles in a chain on the magnetic induced shear odulus is quantitatively studied. When the ratio is large, the multi-chain model is compatible with the single chain model, but when the ratio is small, the difference of the two models is significant and can not be neglected. Making certain the size of the columns and the distance between adjacent columns, after constructing the computational model of BCT structures, the mechanical property of the magnetorheological elastomers composed of columnar structures is analyzed. Results show that, conventional point dipole model has overrated the magnetic-induced shear modulus of the magnetorheological elastomers. From the point of increasing the magnetic-induced shear modulus, when the particle volume fraction is small, the chain-like structure exhibits better result than the columnar structure, but when the particle volume fraction is large,the columnar structure will be better.     

Damping of Magnetorheological Elastomers

The damping property of magnetorheological (MR) elastomers is characterized by a modified dynamic mechanical-magnetic coupled analyzer. The influences of the external magnetic flux density, damping of the matrix, content of iron particles, dynamic strain, and driving frequency on the damping properties of MR elastomers were investigated experimentally. The experimental results indicate that the damping properties of MR elastomers greatly depend on the interfacial slipping between the inner particles and the matrix. Different from general composite materials, the interfacial slipping in MR elastomers is affected bythe external applied magnetic field.     

Effect of carbon black on the mechanical performances of magnetorheological elastomers

Several magnetorheological elastomer (MRE) samples, with different weight percentages of carbon black, were fabricated under a constant magnetic field. Their microstructures were observed by using an environmental scanning electron microscope (SEM), and their mechanical performance including magnetorheological (MR) effect, damping ratio and tensile strength were measured with a dynamic mechanical analyzer (DMA) system and an electronic tensile machine. The experimental results demonstrate that carbon black plays a significant role in improving the mechanical performance of MR elastomers. Besides the merits of high MR effect and good tensile strength, the damping ratio of such materials is much reduced. This is expected to solve a big problem in the application of MR elastomers in practical devices, such as in adaptive tuned vibration absorbers.     

Enhancement in Magnetorheological Effect of Magnetorheological Elastomers by Surface Modification of Iron Particles

In order to obtain magnetorheological (MR) elastomers with high magnetorheological effect, a family of anisotropic rubber-based MR elastomers was developed using a new form of chemical modification. Three different kinds of surfactants, i.e. anionic, nonionic and compound surfactants, were employed separately to modify iron particles. The MR effect was evaluated by measuring the dynamic shear modulus of MR elastomer with a magneto-combined dynamic mechanical analyzer. Results show that the relative MR effect can be up to 188% when the iron particles are modified with 15% Span 80. Besides the surface activity of Span 80, however, such high modifying effect is partly due to the plasticizing effect of Span 80. Compared with the single surfactant, the superior surface activity of compound surfactant makes the relative MR effect reach 77% at a low content of 0.4%. Scanning electron microscope observation shows that the modification of compound surfactant results in perfect compatibility between particles and rubber matrix and special self-assembled structure of particles. Such special structure has been proved beneficial to the improvement of the relative MR effect.     

On the relevance of the 8‐chain model and the full‐network model for the deformation and failure of networks formed through photopolymerization of multifunctional monomers

Crosslinked networks were synthesized by copolymerization of mono‐functional tert‐butyl acrylate (tBA) with diethyleneglycol dimethacrylate (DEGDMA) or polyethylene glycol dimethacrylates (PEGDMA). By varying the chain length and concentration of the difunctional PEGDMA, we obtained tBA‐PEGDMA copolymer networks while by varying the concentration of difunctional DEGDMA, we obtained tBA‐DEGDMA crosslinked networks. The various materials were submitted to large deformations through uniaxial tension tests. For moderate weight percent of crosslinking agent, up to 20%, the networks showed standard S‐shape stress–strain curves, characteristic of rubber‐like elasticity. Two macromolecular models, the 8‐chain model and the full‐network model, were applied to fit the uniaxial tensile response of the materials. Both models provide good representations of the overall uniaxial stress–strain response of each material. After fitting to stress–strain data, the network models were employed to predict the shear modulus and the elongation at break. Neither the 8‐chain nor the full network model were capable of predicting the failure strain or shear modulus, indicating these models are best used to describe stress–strain relations rather than predict mechanical properties for the network polymers considered here. © 2008 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 1226–1234, 2008     

Theoretical modeling of the relationship between Young's modulus and formulation variables for segmented polyurethanes

We describe a new modeling approach to prediction of Young's modulus of segmented polyurethanes. This approach combines micromechanical models with thermodynamic considerations based on the theory of block copolymers. The resulting model predicts both the equilibrium morphology and the “ideal” Young's modulus of a segmented polyurethane polymer as a function of its formulation (hard segment chemical structure, hard segment weight fraction, soft segment equivalent weight) and temperature. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 2123–2135, 2007     

Magneto‐sensitive Elastomers in a Homogeneous Magnetic Field: A Regular Rectangular Lattice Model

A theory of mechanical behaviour of the magneto‐sensitive elastomers is developed in the framework of a linear elasticity approach. Using a regular rectangular lattice model, different spatial distributions of magnetic particles within a polymer matrix are considered: isotropic, chain‐like and plane‐like. It is shown that interaction between the magnetic particles results in the contraction of an elastomer along the homogeneous magnetic field. With increasing magnetic field the shear modulus, G, for the shear deformation perpendicular to the magnetic field increases for all spatial distributions of magnetic particles. At the same time, with increasing magnetic field the Young's modulus, E, for tensile deformation along the magnetic field decreases for both chain‐like and isotropic distributions of magnetic particles and increases for the plane‐like distribution of magnetic particles.

     

Determination of reliable fatigue life predictors for magnetorheological elastomers under dynamic equi-biaxial loading

Fatigue life prediction is of great significance in ensuring magnetorheological elastomer (MRE) based rubber components exhibit reliability and do not compromise safety under complex loading, and this necessitates the development of plausible fatigue life predictors for MREs. In this research, silicone rubber based MREs were fabricated by incorporating soft carbonyl iron magnetic particles. Equi-biaxial fatigue behaviour of the fabricated MREs was investigated by using the bubble inflation method. The relationship between fatigue life and maximum engineering stress, maximum strain and strain energy density were studied. The results showed that maximum engineering stress and stored energy density can be used as reliable fatigue life predictors for SR based MREs when they are subjected to dynamic equi-biaxial loading. General equations based on maximum engineering stress and strain energy density were developed for fatigue life prediction of MREs.     

An experimental investigation of fracture by cavitation of model elastomeric networks

A new methodology to investigate the failure of elastomers in a confined geometry has been developed and applied to model end-linked polyurethane elastomers. The experimental in situ observations show that the elastomers fail by the growth of a single cavity nucleated in the region of maximum hydrostatic stress. Tests carried out at different temperatures for the same elastomer show that the critical stress at which this crack grows is not proportional to the Young's modulus E but depends mainly on the ratio between the mode I fracture energy G_IC and E. A reasonable fit of the data can be obtained with a model of cavity expansion by irreversible fracture calculating the energy release rate by finite elements with a strain hardening constitutive equation. Comparison between different elastomers shows that the material containing both entanglements and crosslinks is both tougher in mode I and more resistant to cavitation relative to its elastic modulus. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48:1409–1422, 2010     

Influence of the crosslink network structure on stress‐relaxation behavior: Viscoelastic modeling of the compression set experiment

A viscoelastic approach of the compression set test is addressed in this work. This test measures the ability of rubber compounds to retain elastic properties after prolonged action of compressive stresses. Elastic properties were tested by recording the normal stress under a constant deformation of 25% with a laboratory rheometer. Considering the Boltzmann superposition principle, compression set data were modeled from the relaxation of Young's modulus, described by a Maxwell spectrum plus a constant E_∞ defining the elastic properties at the long times. This approach was developed with the copolymer of ethylene and vinyl acetate (EVA) networks crosslinked by radical chemistry and by an exchange reaction between acetate groups and silane compounds as crosslinking agents. Regarding the recovery of the elastic properties, radical chemistry provided better results than the exchange reaction for the identical crosslinking density of the network. Then, the Curro–Pincus molecular approach was developed to understand the influence of the microstructure of the EVA network on the elastic properties. The difference of the elastic properties between the two networks crosslinked by two different chemistry means was accounted for by considering the probability of having a dangling end of n units for a random crosslinking process. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1779–1790, 2003     

The evaluation and implementation of magnetic fields for large strain uniaxial and biaxial cyclic testing of Magnetorheological Elastomers

Magnetorheological Elastomers (MREs) are “smart” materials whose physical properties are altered by the application of magnetic fields. In previous studies the properties of MREs have been evaluated under a variety of conditions, however little attention has been paid to the recording and reporting of the magnetic fields used in these tests [1]. Currently there is no standard accepted method for specifying the magnetic field applied during MRE testing. This study presents a detailed map of a magnetic field applied during MRE tests as well as providing the first comparative results for uniaxial and biaxial testing under high strain fatigue test conditions. Both uniaxial tension tests and equi-biaxial bubble inflation tests were performed on isotropic natural rubber MREs using the same magnetic fields having magnetic flux densities up to 206 mT. The samples were cycled between pre-set strain limits. The magnetic field was switched on for a number of consecutive cycles and off for the same number of following cycles. The resultant change in stress due to the application and removal of the magnetic field was recorded and results are presented.     

Effect of solvent on the gelation properties of a metallo-organic polymer of [Fe(II) (4-octadecyl-1,2,4-triazole)3(ClO4)2]n

In this contribution we report on the preparation of thermally responsive supramolecular gels obtained through self-assembling of metallo-organic polymers of lipophilic Fe(II) complexes of 1,2,4-triazole functionalized with octadecyl chains ([Fe(II) (4-octadecyl-1,2,4-triazole)₃(ClO₄)₂]_n) in three organic solvents: toluene, cis-decalin and trans-decalin. A gel phase is formed in these solvents by cooling the homogeneous complex solutions below a well-defined temperature, the so-called gelation threshold. These gels are reversible as they form homogeneous solutions upon heating above the melting temperature. The systems have been characterized for their thermal and viscoelastic properties through differential scanning calorimetry and rheological experiments, respectively. The effect of the solvent type and concentration on the gelation behaviour of the metallo-organic polymer has been analysed. The results obtained point to structural differences and different gelation mechanisms for the gels prepared in different solvents and they also suggest the possibility to control the spin-crossover transition temperature associated to the sol-gel transition.     

Kinetics of solvent absorption and permeation through a highly swellable elastomeric network

To model a polymer gel or an elastomer undergoing a large change in volume under the action of a solvent diffusing in or out of it, a theoretical approach based on an elastohydrodynamic point of view is proposed. Drawing a parallel between the polymer network/solvent system of interest and a liquid flowing through a porous medium, the friction between the polymer and the solvent is described phenomenologically. An equation that couples the large elastic deformations undergone by the polymer network and the diffusion process is derived and then solved numerically in various cases. Special emphasis is placed on the influence of the shear elasticity during the diffusion process. During the swelling process, a nonzero shear modulus induces a nonisotropic swelling at the surface that is responsible for the “sigmoidal” shape of the mass uptake of solvent with the square root of time, as well as for the presence of a “front” in the concentration profile when the solvent advances inside the network. In a permeation process, the solvent flux deviates from its linear behavior as soon as a nonnegligible deformation of the membrane is present. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 166–182, 2003     

多相高分子体系中的粘弹相分离行为

相分离广泛存在于各种凝聚态物质中.根据局部浓度的变化形式,可将相分离分为固体模型(model B)和流体模型(model H),这两种模型适用于动力学对称的体系.近年来,Tanaka发现在一些动力学不对称的多组分高分子体系里存在一种新的相分离模式,其相分离过程分为动力学过程可用一个普适的粘弹模型来进行描述.动力学不对称可由体系中两组分间大的尺寸差异或玻璃化温度差异引起.本文介绍了多相高分子体系中产生粘弹相分离的原理及其基本特征,并讨论了模量、粘度、填料等因素对粘弹相分离动力学过程及多相体系微观结构的影响.     

Low‐temperature route to thermoplastic polyamide elastomers

Thermoplastic polyamide elastomers were obtained by polymerization of aminobenzoyl‐substituted telechelics derived from poly(tetrahydrofuran)‐diols (number‐average molecular weight: 1400 or 2000 g mol^?1) with several diacid dichlorides (terephthaloyl dichloride, 4,4′‐biphenyldicarbonyl dichloride, or 2,6‐naphthalenedicarbonyl dichloride) and chlorotrimethylsilane in N,N‐dimethylacetamide at 0–20 °C. The as‐prepared polymers had melting temperatures above 190 °C and exhibited elastic properties at room temperature, as evidenced by dynamic mechanical analysis and stress–strain measurements. The polymer with 2,6‐naphthalenedicarboxamide hard segments had the widest rubbery plateau within the series, the highest extension at break, and good recovery properties. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1449–1460, 2004     

Determination of the dynamic complex modulus of viscoelastic materials using a time domain approach

Viscoelastic and poroelastic materials are widely used in multilayer panels for noise control. They are usually used as an inner decoupling layer in double wall systems in order to increase the sound transmission loss of a bare plate. In order to correctly simulate the acoustical behaviour of such systems, it is necessary to measure the elastic parameters of these materials (storage and loss moduli, and Poisson's ratio). Physical properties related to pore morphology also need to be determined for open cell structures. Most of the materials used in trimmed panels can show elastic parameters that vary with frequency, thus a quasi-static measurement technique is not accurate enough to consider such viscoelasticity effects. This paper focuses on the estimation of complex modulus as a function of the frequency of isotropic viscoelastic materials. In particular, the tested material is positioned between two plates, with one of them being excited by an electromagnetic shaker. Using a sine burst as an excitation signal, the accelerometric response in the time domain is measured at the top and bottom plates. The time of flight between the plates and the envelope function of time domain acceleration at the top plate are then found. A transfer matrix model of the experimental setup is used to inversely estimate the complex modulus of the materials once the remaining mechanical and physical properties have been fixed. The results will be presented and discussed for different materials and compared with well-established quasi-static and dynamic techniques.     

Mechanical and thermo‐mechanical studies of double networks based on thermoplastic elastomers

A new approach to prepare and characterize double network elastomeric systems was investigated. A styrene‐ethylene‐co‐butylene‐styrene (SEBS) triblock copolymer system containing physical crosslinks was used to achieve a double network by additional crosslinking using ultra‐violet (UV) light. An ethylene–propylene–diene monomer (EPDM) terpolymer system containing chemical crosslinks was used to achieve a conventional double network using UV crosslinking. Properties from conventional monotonic tensile tests, dynamic mechanical analysis, and thermomechanical properties were investigated. These double network elastomers show a transition between competitive and collaborative behavior in their mechanical properties and lower coefficients of thermal expansion arising from a competition of the networks. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 778–789, 2010