Mechanical switching of ferro-electric rubber

At the A to C transition, smectic elastomers have recently been observed to undergo $\sim$35% spontaneous shear strains. We first explicitly describe how strains of up to twice this value could be mechanically or electrically induced in Sm-$C$ elastomers by rotation of the director on a cone around the layer normal at various elastic costs depending on constraints. Secondly, for typical sample geometries, we give the various microstructures in Sm-$C$ akin to those seen in nematic elastomers under distortions with constraints. It is possible to give explicit results for the nature of the textures. Chiral Sm-$C$ elastomers are ferro-electric. We calculate how the polarization could be mechanically reversed by large, hard or soft strains of the rubber, depending upon sample geometry.Comment: 15 pages, 12 figure

Hydrogen bonded supramolecular elastomers : correlating hydrogen bonding strength with morphology and rheology

A series of six low molecular weight elastomers with hydrogen bonding end-groups have been designed, synthesised and studied. The poly(urethane) based elastomers all contained essentially the same hard block content (ca. 11%) and differ only in the nature of their end-groups. Solution state 1H NMR spectroscopic analysis of model compounds featuring the end-groups demonstrate that they all exhibit very low binding constants, in the range 1.4 to 45.0 M-1 in CDCl3, yet the corresponding elastomers each possess a markedly different nanoscale morphology and rheology in the bulk. We are able to correlate small variations of the binding constant of the end-groups with dramatic changes in the bulk properties of the elastomers. These results provide an important insight into the way in which weak non-covalent interactions can be utilized to afford a range of self-assembled polyurethane based materials that feature different morphologies

Perfluoroether triazine elastomers

The synthesis of high performance elastomers with the high thermal stability and chemical, inertness of perfluoroalkylene triazine and a low glass transition temperature is discussed. Perfluorether triazine elastomers were proposed as potentially superior. It is concluded that the difficulties experienced in fluoroalkytriazine elastomer synthesis can be overcome by a four-step reaction process involving chain extension, triazine ring closure, crosslinking, and elastomer curing. Molecular weight can be controlled in the initial polymer formation so that elastomer modulus can be determined. The final product elastomers exhibit a useful elastomeric range of approximately 45 to 325 C with an oxidative stability superior to other broad range elastomers

Structure and dielectric properties of electroactive tetraaniline grafted non-polar elastomers

Intrinsic modification of polybutadiene and block copolymer styrene–butadiene–styrene with the electrically conducting emeraldine salt of tetraaniline (TANI) via a three-step grafting method, is reported in this work. Whilst the TANI oligomer grafted at a similar rate to both polybutadiene and styrene–butadiene–styrene under the same conditions, the resulting elastomers exhibited vastly different properties. 1 mol% TANI-PB exhibited an increased relative permittivity of 5.9, and a high strain at break of 156%, whilst 25 mol% TANI-SBS demonstrated a relative permittivity of 6.2 and a strain at break of 186%. The difference in the behaviour of the two polymers was due to the compatibilisation of TANI by styrene in SBS through π-π stacking, which prevented the formation of a conducting TANI network in SBS at. Without the styrene group, TANI-PB formed a phase separated structure with high levels of TANI grafting. Overall, it was concluded that the polymer chain structure, the morphology of the modified elastomers, and the degree of grafting of TANI, had the greatest effect on the mechanical and dielectric properties of the resultant elastomers. This work paves the way for an alternative approach to the extrinsic incorporation of conducting groups into unsaturated elastomers, and demonstrates dielectric elastomers with enhanced electrical properties for use in actuation devices and energy harvesting applications

Elasticity of Polydomain Liquid Crystal Elastomers

We model polydomain liquid-crystal elastomers by extending the neo-classical soft and semi-soft free energies used successfully to describe monodomain samples. We show that there is a significant difference between polydomains cross-linked in homogeneous high symmetry states then cooled to low symmetry polydomain states and those cross-linked directly in the low symmetry polydomain state. For example, elastomers cross-linked in the isotropic state then cooled to a nematic polydomain will, in the ideal limit, be perfectly soft, and with the introduction of non-ideality, will deform at very low stress until they are macroscopically aligned. The director patterns observed in them will be disordered, characteristic of combinations of random deformations, and not disclination patterns. We expect these samples to exhibit elasticity significantly softer than monodomain samples. Polydomains cross-linked in the nematic polydomain state will be mechanically harder and contain characteristic schlieren director patterns. The models we use for polydomain elastomers are spatially heterogeneous, so rather than solving them exactly we elucidate this behavior by bounding the energies using Taylor-like (compatible test strain fields) and Sachs (constant stress) limits extended to non-linear elasticity. Good agreement is found with experiments that reveal the supersoft response of some polydomains. We also analyze smectic polydomain elastomers and propose that polydomain SmC* elastomers cross-linked in the SmA monodomain state are promising candidates for low field electrical actuation.Comment: 13 pages, 11 figure

Prepolymer dianhydrides

A process for preparing dianhydrides that are miscible with hydroxyl prepolymers at moderate temperatures and can cure hydroxyl prepolymers to elastomers at moderate temperatures is disclosed. The dianhydrides are prepared by solution reaction of a prepolymer diol with excess hydride followed by removal of unreacted dianhydride. The prepolymer dianhydrides are miscible with hydroxyl substituted hydrocarbon prepolymers and cure the prepolymers to polyester-linked elastomers