Abstract
The present paper deals with the results of an orientating, quantitative investigation of sulfur vulcanization accelerated by thiuram disulfide, with tetramethylthiuram disulfide as the representative example. It was found: In the sulfur cure of natural rubber with tetramethylthiuram disulfide at different TMTD:S ratios, the rates of TMTD decrease and dithiocarbamate formation increase with increasing sulfur concentration, the TMTD content being kept constant. The rates practically do not change any further when the compounds contain 6 gram atoms of sulfur per mole of thiuram disulfide. The peak value of dithiocarbamate formation increases with the increase of sulfur concentration and reaches a constant end value of about 90 mole per cent based on the amount of original thiuram disulfide, when the stocks contain 4 gram atoms of sulfur per mole thiuram disulfide. This end value is identical to the end value of dithiocarbamate formation in the reaction of thiuram disulfide with zinc oxide (in the absence of rubber). The crosslinking, as measured by the change of reciprocal equilibrium swelling per time unit is also a reaction whose rate increases with the sulfur concentration to the point where the compounds contain 6 gram atoms of sulfur per mole of thiuram disulfide. The optimum degrees of crosslinking are roughly proportional to the sulfur concentration; at high sulfur levels the vulcanizates tend to revert. As in the pure TMTD vulcanization, the TMTD decrease as well as the dithiocarbamate formation are always first order reactions. The reversion at higher sulfur levels as well as the complicated course of the increase of combined sulfur during vulcanization render all but impossible an accurate determination of the reaction order for the crosslinking at higher sulfur levels. Nevertheless, in vulcanizations with 1 mole TMTD per 1 or 2 gram atoms of sulfur the crosslinking is a first order reaction.
A general expression for coupled enzyme assays of hysteretic enzymes
