Phenothiazine as an Antifatigue Agent for Natural Rubber, Synthetic Polyisoprene and SBR

1965 ◽  
Vol 38 (3) ◽  
pp. 661-665
Author(s):  
Z. N. Tarasova ◽  
I. I. Eitingon ◽  
L. G. Senatorskaya ◽  
T. V. Fedorova ◽  
B. A. Dogadkin

Abstract Phenothiazine has no effect on vulcanization of rubber or standard mechanical properties of the vulcanizates. Phenothiazine considerably increases fatigue resistance of vulcanizates of the rubbers studied, under different fatigue conditions. Under the effect of thermal oxidation and repeated deformation phenothiazine or its conversion products combine with the vulcanizate. The phenothiazine does not combine when subjected only to heating. When used with certain inhibitors of oxidation phenothiazine has a synergistic effect.

2014 ◽  
Vol 1073-1076 ◽  
pp. 12-15 ◽  
Author(s):  
Ke Chen ◽  
Rui Wang

The natural rubber/polyvinyl alcohol (NR/PVA) blends containing epoxid natural rubber as the compatilizer were prepared using latex compounding techniques. The mechanical and thermal oxidation aging properties were studied. Mechanical test showed that the tear strength and hardness of the NR were significantly improved due to adding of the PVA. The tensile strength decreased significantly along with the PVA increasing. Thermal oxidation aging test had obviously impact on the mechanical properties of the material. The performance retention of the material properties was taken effect significantly on the aging test.


2012 ◽  
Vol 85 (1) ◽  
pp. 120-131 ◽  
Author(s):  
Md. Najib Alam ◽  
Swapan Kumar Mandal ◽  
Subhas Chandra Debnath

Abstract Several zinc dithiocarbamates (ZDCs) as accelerator derived from safe amine has been exclusively studied in the presence of thiazole-based accelerators to introduce safe dithiocarbamate in the vulcanization of natural rubber. Comparison has been made between conventional unsafe zinc dimethyldithiocarbamate (ZDMC) with safe novel ZDC combined with thizole-based accelerators in the light of mechanical properties. The study reveals that thiuram disulfide and 2-mercaptobenzothiazole (MBT) are always formed from the reaction either between ZDC and dibenzothiazyledisulfide (MBTS) or between ZDC and N-cyclohexyl-2-benzothiazole sulfenamide (CBS). It has been conclusively proved that MBT generated from MBTS or CBS reacts with ZDC and produces tetramethylthiuram disulfide. The observed synergistic activity has been discussed based on the cure and physical data and explained through the results based on high-performance liquid chromatography and a reaction mechanism. Synergistic activity is observed in all binary systems studied. The highest tensile strength is observed in the zinc (N-benzyl piperazino) dithiocarbamate-accelerated system at 3:6 mM ratios. In respect of tensile strength and modulus value, unsafe ZDMC can be successfully replaced by safe ZDCs in combination with thiazole group containing accelerator.


Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1510
Author(s):  
Marek Pöschl ◽  
Shibulal Gopi Sathi ◽  
Radek Stoček ◽  
Ondřej Kratina

The rheometer curing curves of neat natural rubber (NR) and neat chloroprene rubber (CR) with maleide F (MF) exhibit considerable crosslinking torque at 180 °C. This indicates that MF can crosslink both these rubbers via Alder-ene reactions. Based on this knowledge, MF has been introduced as a co-crosslinking agent for a 50/50 blend of NR and CR in conjunction with accelerated sulfur. The delta (Δ) torque obtained from the curing curves of a blend with the addition of 1 phr MF was around 62% higher than those without MF. As the content of MF increased to 3 phr, the Δ torque was further raised to 236%. Moreover, the mechanical properties, particularly the tensile strength of the blend with the addition of 1 phr MF in conjunction with the accelerated sulfur, was around 201% higher than the blend without MF. The overall tensile properties of the blends cured with MF were almost retained even after ageing the samples at 70 °C for 72 h. This significant improvement in the curing torque and the tensile properties of the blends indicates that MF can co-crosslink between NR and CR via the Diels–Alder reaction.


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