TETRAMETHYLTHIURAM DISULFIDE AND 2-MERCAPTOBENZOTHIAZOLE AS BINARY ACCELERATORS IN SULFUR VULCANIZATION .3. VULCANIZATION OF POLYISOPRENE IN THE ABSENCE OF ZNO
Bvkm. Giuliani et Wj. Mcgill, TETRAMETHYLTHIURAM DISULFIDE AND 2-MERCAPTOBENZOTHIAZOLE AS BINARY ACCELERATORS IN SULFUR VULCANIZATION .3. VULCANIZATION OF POLYISOPRENE IN THE ABSENCE OF ZNO, Journal of applied polymer science, 62(7), 1996, pp. 1057-1066
Polyisoprene was vulcanized with the binary accelerator system tetrame
thylthiuram di-sulfide-2-mercaptobenzothiazole (TMTD-MBT) in the absen
ce of ZnO. Samples were heated in a DSC at a programmed rate, the reac
tion was stopped at points along the thermal curve, and the system was
analyzed. Extractable curatives and reaction intermediates were analy
zed by HPLC and the crosslink density of samples measured by swelling.
Two crosslinking reaction sequences were identified, the first being
initiated by polysulfides of the mixed accelerator N,N-dimethyldithioc
arbamylbenzothiazole disulfide, and the second by MET. All the TMTD is
consumed in the first reaction sequence. Synergism of the reaction is
discussed in terms of recent work detailing a reaction mechanism for
TMTD-accelerated vulcanization. (C) 1996 John Wiley & Sons, Inc.