6.2 Rubber Reinforcement by In Situ Silica
111
Fig. 6.2 Sol–gel reaction of tetraethoxysilane to produce silica
Mechanical mixing
Swelling
Drying
Vulcanization
in situ Sol-gel reaction
Raw rubber
Rubber vulcanizate
in situ Silica loaded rubber
Curing reagents
TEOS, Catalyst
Fig. 6.3 Preparation of in situ silica/rubber composite from rubber vulcanizate prepared by the
conventional rubber processing (Method A). TEOS designates tetraethoxysilane
On the resultant in situ silica/rubber composites prepared by Method A, structure and properties have been studied extensively. In this section, those of IR (isoprene rubber, also called synthetic natural rubber) cross-linked by peroxide are to be
described. The rubber specimen is one of the simplest: The peroxide cross-linking
is much simpler than sulfur/accelerator system for vulcanization, which necessitates
mixing of several curing reagents. In addition, IR is free from naturally produced
non-rubber components like proteins, while natural rubber (NR) may contain a few
percent of non-rubber constituents.
Figure 6.4 shows conventional TEM image of in situ silica in cross-linked IR,
whose silica contents are equivalent to 22 phr [55]. The averaged radius of the
silica generated in situ is approximately 34 nm, and it is noticeable that spherical
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