Electrical and mechanical property tests have been used to examine the changes in the carbon black network structure that occur in a filled elastomer at large strains in tension and compression. These changes have been examined both in materials that have no previous loading history and in test pieces that have been subjected to a specific known prestrain. When a previously unstrained, filled elastomer specimen is stretched to moderate extensions, the electrical resistivity increases. This is ascribed to the breakdown of the carbon black network structure. At higher tensile extensions, the resistivity decreases. This reduction in the electrical resistivity is attributed to the alignment of the shaped carbon black aggregates under strain. During unloading, the resistivity behavior is different from that during loading, with the final unloaded electrical resistivity being significantly higher than that measured in the unstrained elastomer. This dramatic change in the electrical properties after unloading is in marked contrast to the relatively modest changes observed in the mechanical behavior. After the first cycle, the electrical behavior becomes much more reversible, and this indicates that the bulk of the damage experienced by the carbon black network is developed during the first cycle. After unloading from a large strain, the electrical anisotropy is small, whereas the mechanical anisotropy is more marked. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 2079–2089, 2003
Oesophageal cancer is the ninth leading cause of malignant cancer death and its prognosis remains poor, ranking as the sixth most frequent cause of death in the world. This research work aims to adopt an Auxetic (rotating-squares) geometry device, that had previously been examined theoretically and analysed by Grima and Evans (J Mater Sci Lett 19(17):1563-1565, 2000), to produce a novel Auxetic oesophageal stent and stent-grafts relevant to the palliative treatment of oesophageal cancer and also for the prevention of dysphagia. This paper discusses the manufacture of a small diameter Auxetic oesophageal stent and stent-graft. The oral deployment of such an Auxetic stent would be simplest if a commercial balloon dilatational catheter was used as this obviates the need for an expensive dedicated delivery system. A novel manufacturing route was employed in this research to develop both Auxetic films and Auxetic oesophageal stents, which ranged from conventional subtractive techniques to a new additive manufacturing method. Polyurethane was selected as a material for the fabrication of Auxetic films and Auxetic oesophageal stents because of its good biocompatibility and non-toxicological properties. The Auxetic films were later used for the fabrication of seamed Auxetic oesophageal stents. The flexible polyurethane tubular grafts were also attached to the inner luminal side of the seamless Auxetic oesophageal stents, in order to prevent tumour in-growth. Scanning electron microscopy was used to conduct surface morphology study by using different Auxetic specimens developed from different conventional and new additive manufacturing techniques. Tensile testing of the Auxetic films was performed to characterise their mechanical properties. The stent expansion tests of the Auxetic stents were done to analyse the longitudinal extension and radial expansion of the Auxetic stent at a range of radial pressures applied by the balloon catheter, and to also identify the pressure values where the Auxetic stent fails. Finite element models of both Auxetic film and Auxetic stent were developed, and the results were compared with experimental results with a good agreement. The tensile testing of the Auxetic polyurethane films revealed that the Poisson's ratio of the sample ranged between -0.87 and -0.963 at different uniaxial tensile load values. From the stent expansion test, it was found that the Auxetic oesophageal stent radially expanded from 0.5 to 5.73 mm and longitudinally extended from 0.15 to 1.83 mm at a range of applied pressure increments (0.5-2.7 bar) from the balloon catheter.
This paper describes the preparation of ceramic foams by expansion of a ceramic suspension based on a polyurethane system. The microstructure and degree of reticulation of the foamed ceramic were examined and analysed with the help of a simple geometrical model. Like the porous ceramics prepared by the replica processing method, these foamed ceramics possess open cells in a nearly equiaxed shape but the cell size is much ®ner. The ratio of the window size to the cell size is a useful parameter for characterising the geometry of the foam and is related to the qualitative concept of degree of reticulation. For a face centred cubic array of cells it is related geometrically to the volume fraction of porosity and this relationship is tested using microstructural measurements for a range of ceramic foams. #
Polydimethylsiloxane (PDMS) hybrid composites consisting of exfoliated graphite nanoplatelets (xGnPs) and multiwalled carbon nanotubes functionalized with hydroxyl groups (MWCNTs-OH) were fabricated, and the effects of the xGnP/MWCNT-OH ratio on the thermal, electrical, and mechanical properties of polydimethylsiloxane (PDMS) hybrid composites were investigated. With the total filler content fixed at 4 wt%, a hybrid composite consisting of 75% × GnP/25% MWCNT-OH showed the highest thermal conductivity (0.392 W/m.K) and electrical conductivity (1.24 × 10-3 S/m), which significantly exceeded the values shown by either of the respective single filler composites. The increased thermal and electrical conductivity found when both fillers are used in combination is attributed to the synergistic effect between the fillers that forms an interconnected hybrid network. In contrast, the various different combinations of the fillers only showed a modest effect on the mechanical behavior, thermal stability, and thermal expansion of the PDMS composite.
The nature of filler−polymer and filler−filler interactions in rubber composites under strain remains an open question in soft matter physics. These interactions are key to explaining the rich variety of complex behavior exhibited by particle-filled rubber products. In this paper we demonstrate a simultaneous dielectric/dynamic mechanical analysis technique (SDMS) which provides new insights into the structure−property relationships of filled rubbers. The complex permittivity of carbon black filled natural rubber has been characterized under a simultaneous tensile strain field (from 0.1% to 50%). The complex permittivity exhibits a dramatic nonlinear dependence on strain coupled with features which are analogous to mechanical strain softening and strain history, namely the "Payne" and "Mullins" effects. The sensitivity of the complex permittivity to such effects is several orders of magnitude greater than in corresponding, traditional mechanical tests. In addition, we demonstrate for the first time that it is possible to use both strain and electrical field frequency as "dipole filters" which can be used to selectively probe the dipoles present at the polymer−filler interface.
Smart heating devices with reliable self-regulating performances and high efficiency, combined with additional properties like mechanical flexibility, are of particular interest in healthcare, soft robotics, and smart buildings. Unfortunately, the development of smart heaters necessitates managing normally conflicting requirements such as good self-regulating capabilities and efficient Joule heating performances. Here, a simple and universal materials design strategy based on a series connection of different conductive polymer composites (CPC) is shown to provide unique control over the pyroresistive properties. Hooke's and Kirchhoff 's laws of electrical circuits can simply predict the overall pyroresistive behavior of devices connected in series and/ or parallel configurations, hence providing design guidelines. An efficient and mechanically flexible Joule heating device is hence designed and created. The heater is characterized by a zero temperature coefficient of resistance below the self-regulating temperature, immediately followed by a large and sharp positive temperature coefficient (PTC) behavior with a PTC intensity of around 10 6 . Flexibility and toughness is provided by the selected elastomeric thermoplastic polyurethane (TPU) matrix as well as the device design. The universality of the approach is demonstrated by using different polymer matrices and conductive fillers for which repeatable results are consistently obtained.the merits of plastics and conductive fillers. [1] Their capability of detecting and responding to external stimuli has offered a range of promising applications by performing both sensing (damage, [2] strain, [3] humidity, [4] vapor, [5] degradation, [6] and current-limiting), [7] and actuating (artificial muscles, [8] and electroactive shape memory) [9] functions. In particular, CPCs are practical choices for pyroresistive applications like self-regulating heaters, temperature sensors, and safe battery switches, due to their capability of changing electrical resistivity upon heating. [10] Since their introduction in the late 1970s, self-regulating heating devices have been widely adopted in applications like domestic heaters and deicing units. These smart heaters can operate at a nearly constant temperature over a broad range of voltage and dissipative conditions by utilizing the positive temperature coefficient (PTC) effect. The PTC effect, where the electrical resistivity increases with increasing operating temperature, is the main property that enables self-regulating heating. [11] The PTC phenomenon is generally explained by the mismatch of thermal expansion between the polymer matrix and the filler. [12] When the temperature increases and exceeds a certain threshold, the continuous network formed by the conductive fillers is disrupted. Due to expansion of the polymer matrix, the electrical conductivity and the current passing through the sample are reduced, regulating the temperature within a desired range. [13] Great efforts have been made to design PTC materials that p...
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