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Dual chlorine/carboxyl cure sites

The dual chlorine/carboxyl cure sites have the capability of using a very wide variety of cure systems and wUl produce compounds with excellent heat resistance... [Pg.157]

New efficient vulcanization systems have been introduced in the market based on quaternary ammonium salts initially developed in Italy (29—33) and later adopted in Japan (34) to vulcanize epoxy/carboxyl cure sites. They have been found effective in chlorine containing ACM dual cure site with carboxyl monomer (43). This accelerator system together with a retarder (or scorch inhibitor) based on stearic acid (43) and/or guanidine (29—33) can eliminate post-curing. More recently (47,48), in the United States a proprietary vulcanization package based on zinc diethyldithiocarbamate [14324-55-1]... [Pg.477]

In order to enhance the reactivity of the chlorine atom, a second reactive monomer can be adopted giving dual cure sites. According to the Hterature, the second monomer can contain carboxyl (22—24), cyanoalkyl (25), hydroxypropyl (26), or epoxy groups (27,28). [Pg.476]


See other pages where Dual chlorine/carboxyl cure sites is mentioned: [Pg.476]    [Pg.161]   


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