In this work a systematic investigation of crosslinking kinetics of Sylgard184 polydimethylsiloxane is performed in both isothermal and dynamic conditions. The results are discussed in terms of two conversions, α_C and α_R determined by thermal and rheological analysis, respectively. Thermal analysis can well detect the first stage of the reaction, while rheological analysis starts being sensitive only at longer time. However, once the rheological response is observable, it changes with time faster than the calorimetric one. From rheology experiments it comes out that the gel point occurs at α_R = 0.53, independently of the applied thermal history. At gel point, α_C is around 0.30 indicating that about 30% of the bonds involved in the crosslinking process is enough to create an infinite network. A modified version of the Kamal's autocatalytic model allows to fit and predict the experimental findings from both the techniques; however, two distinct sets of parameters have been used. The results of this work may be a useful tool to design appropriate curing cycles for the preparation of Sylgard184.

With a view toward the application of highly hygroscopic polymers as a humidity responsive self-actuator, the evaluation of the real time moisture concentration in the material becomes a priority. In this paper, the moisture diffusion process in a cellulose acetate (53.3% of acetylation) has been studied. Membranes of cellulose acetate (thickness within the range 66–200 µm) have been prepared, and the moisture absorption at room temperature and at a different relative humidity (RH within the range 21–53%) has been monitored. An analytical model has been used to describe the observed non-Fickian sigmoidal behavior of moisture diffusion. A relaxation factor (β) of about 0.026 s⁻¹and a moisture diffusion coefficient (D) of 3.35 × 10^–6mm²/s have been determined. At constant room temperature, the moisture concentration at saturation (C_sat) has shown a linear relation with relative humidity. The identified values β, D and C_satof the analytical model have been used as input for the finite element simulation of the non-Fickian diffusion. The reliability of the finite element simulations has been confirmed with a second set of experiments.

The aim of this work was to analyze the influence of fibers on the mechanical behavior of fiber-reinforced elastomers under cyclic loading. Thus, the focus was on the characterization of structure–property interactions, in particular the dynamic mechanical and viscoelastic behavior. Endless twill-woven glass fibers were chosen as the reinforcement, along with silicone as the matrix material. For the characterization of the flexible composites, a novel testing device was developed. Apart from the conventional dynamic mechanical analysis, in which the effect of the fiber orientation was also considered, modified step cycle tests were conducted under tensile loading. The material viscoelastic behavior was studied, evaluating both the stress relaxation response and the capability of the material to dissipate energy under straining. The effects of the displacement rate of the strain level, the amplitude of the strain applied in the loading–unloading step cycle test, and the number of the applied cycles were evaluated. The results revealed that an optimized fiber orientation leads to 30-fold enhanced stiffness, along with 10 times higher bearable stress. The findings demonstrated that tailored reinforced elastomers with endless fibers have a strong influence on the mechanical performance, affecting the structural properties significantly.

The fracture behavior of carbon black‐filled natural rubber compounds, differing in filler content, was studied performing tensile tests in biaxial loading conditions, using a central notched cross‐shaped specimen. The test consisted of two steps: a drawing step was initially performed loading the specimen in the direction parallel to the notch plane, up to different draw ratios, and then the specimen was loaded in the direction normal to the notch plane up to fracture. Using a fracture mechanics approach, the fracture toughness was evaluated as a function of the draw ratio applied in the drawing step. A correlation between the fracture phenomenology observed and molecular orientability and orientation was attempted. © 2010 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 48: 1509–1515, 2010