Viscoelastic properties of colloidal systems with attractive solid particles at low concentration: A review, new results and interpretations.

This paper concerns the viscoelastic properties and the resulting structure of colloidal systems with short-range attractions in the regime where the volume fraction f is small. Unlike the high ϕ regime, which is well understood in terms of mode-coupling theory (MCT), the low ϕ regime is still the subject of a debate based on different concepts such as percolation, diffusion-limited colloidal aggregation (DLCA), jamming, or cluster mode-coupling approach. Prior to the analysis of three examples of attractive systems at low ϕ values, a summary of concepts relevant to understanding the formation and properties of such attractive particles is discussed in the present study.

Main-chain liquid-crystal elastomers versus side-chain liquid-crystal elastomers: similarities and differences in their mechanical properties.

After a general introduction on the main aspects of the mechanical properties of main-chain liquid-crystal elastomers (MCLCEs) and side-chain liquid-crystal elastomers (SCLCEs), new results will be presented dealing with several MCLCEs with a cross-linker density C = 8%, 6% and 4% and with a SCLCE with C = 10%, all prepared by the two-step cross-linking process. A non-SCLCE with bulky side-groups similar in shape to the mesogens was also synthesized for comparison with the SCLCE. Most of the experiments were performed with a piezorheometer allowing the determination of the shear anisotropy of the samples by applying shear in a direction parallel or perpendicular to the director, and with a thermo-elastic device for the E measurements.

Motorizing fibres with geometric zero-energy modes.

Responsive materials have been used to generate structures with built-in complex geometries, linear actuators and microswimmers. These results suggest that complex, fully functional machines composed solely from shape-changing materials might be possible . Nonetheless, to accomplish rotary motion in these materials still relies on the classical wheel and axle motifs.

Mechanical properties of monodomain nematic side-chain liquid-crystalline elastomers with homeotropic and in-plane orientation of the director.

We present the first study of the shear mechanical properties of monodomain nematic side-chain liquid-crystal elastomers (SCLCEs) prepared by cross-linking with UV irradiation a nematic side-chain liquid-crystal polymer oriented with an electric or a magnetic field. Their elastic behavior was studied in the dry, swollen and stretched states, in order to check the various theoretical descriptions of these systems. The shear measurements taken on the dry samples show that the shear anisotropy is much smaller than that of the usual twice cross-linked samples oriented by a mechanical stretching of the network formed after the first cross-linking step, demonstrating that the elasticity of the networks strongly depends on the preparation procedure used.

Gel-like elasticity in glass-forming side-chain liquid-crystal polymers.

We study the complex shear modulus G of two side-chain liquid-crystal polymers (SCLCPs), a methoxy-phenylbenzoate substituted polyacrylate (thereafter called PAOCH3 ), and a cyanobiphenyl substituted polyacrylate supplied by Merck (thereafter called LCP105) using a piezoelectric rheometer. Two methods of filling the cell are used: (a) a capillary method, which can be used only at high temperature because of the low value of the viscosity, and (b) the classical one, thereafter called compression method, which consists in placing the sample between the two slides of the cell and to bring them closer. By filling the cell at high temperature either with the compression or the capillary method, we show that the response of both compounds is liquidlike ( G' approximately f2 and G'' approximately f , where f is the frequency) for temperatures higher than a certain temperature T0 and gel-like (G' approximately const, G'' approximately f) below T0.