Abstract
The reactions of rubber with aldehydes have previously been studied in latex or in solutions and the reaction products formed by cyclization, condensation, or addition, have been reported. In the present study, solid-state reactions of rubber with aldehydes were carried out. It was found that crosslinked rubbers may be obtained by press curing in the presence of aldehydes with acidic catalysts. Poly-chloroprene and Hypalon especially undergo these reactions without a catalyst or with a small amount of catalyst. In the experiments using various aldehydes, some improvements in the properties of the crosslinked rubber were observed when aldehydes such as paraformaldehyde or α-polyoxymethylene were used. Some Lewis acids such as SnCl2·2H2O were found to be more effective catalysts than the above, and it was found that organic acids such as p-toluenesulfonic acid could also be used. The curing seemed to be an ionic reaction. The physical properties of the crosslinked rubber are similar to those of sulfur-cured rubbers.
Ionic Conduction through Reaction Products at the Electrolyte–Electrode Interface in All-Solid-State Li+ Batteries
