Mechanism of Rubber Vulcanization with Sulfur

1938 ◽  
Vol 11 (1) ◽  
pp. 107-130
Author(s):  
W. K. Lewis ◽  
Lombard Squires ◽  
Robert D. Nutting

Abstract THAT vulcanization of rubber with sulfur always involves a chemical reaction consisting in the addition of sulfur to the double bonds of the rubber molecule has been conclusively established (18, 28). The facts indicate that this addition of sulfur to rubber is an irreversible reaction (31). The temperature coefficient of the reaction is high, increasing about 2.65 fold per 10° C. at ordinary curing temperatures (31). Furthermore, the reaction is apparently exothermic (4, 24). It is noteworthy that catalysts are apparently necessary, since synthetic rubbers prepared from pure materials add sulfur slowly, if at all. The proteins and perhaps the resins in natural rubber undoubtedly serve as accelerators. The curves for combined sulfur vs. time of cure for typical mixes are shown in Figures 1 and 2. Figure 1 is taken from the data of Kratz and Flower (16); the composition and temperature of cure for this mix are shown in Cranor's Table I (9). Figure 2, curve 1, is from Table I of Eaton and Day (10), and curve 2 from data obtained in this laboratory (27, Table I). Superficial inspection of these curves shows extraordinary divergence of type. Figure 1 is a typical fadeaway curve, characteristic of most chemical reactions, where the reaction rate decreases with decreasing concentration of the reacting materials. Curve 1, Figure 2, is an entirely different type, where the rate of sulfur addition is constant until nearly 70 per cent of the initial sulfur has reacted. Curve 2, Figure 2, shows even more complex behavior. Again the rate is constant in the initial portions of the cure. However, following this period, the rate increases markedly but later falls off, approaching zero, to give an S-shaped eurve.

1946 ◽  
Vol 19 (3) ◽  
pp. 534-545
Author(s):  
Max H. Keck ◽  
La Verne E. Cheyney

Abstract In conclusion, the data presented here indicate that two types of chemical reactions take place during the vulcanization of Buna-S stocks of a specific type: (1) a combination with sulfur, which may or may not involve the double bonds in the polymer, and which may be similar in character to the primary vulcanization reaction of natural rubber; (2) a second reaction, presumably polymerization, which accompanies the first and is related to and possibly initiated by it, and which continues on over cure.


1908 ◽  
Vol 8 (4) ◽  
pp. 536-542 ◽  
Author(s):  
Herbert Edmeston Watson

In a recent paper by Miss Chick on “The Laws of Disinfection”, it was pointed out that disinfection of bacteria is strictly analogous to a chemical reaction in which individual bacteria play the part of molecules. Thus, if n be the number of bacteria present at any time t during dis-infection, , where K is a constant. Also, if K1, K2 are these constants for two different temperatures is also constant, i.e. Arrhenius' formula for the temperature coefficient of chemical reactions holds good in the case of bacteria as well. In addition to this, it was found that the relation between the concentration of the disinfectant and the time of disinfection (that is, the time required to reduce the original number of bacteria by a given percentage) might abe approximately expressed by the empirical lawwhere C is the concentration at time t.


2013 ◽  
Vol 04 (supp01) ◽  
pp. 1341001 ◽  
Author(s):  
TOMOAKI WATANABE ◽  
YASUHIKO SAKAI ◽  
KOUJI NAGATA ◽  
OSAMU TERASHIMA ◽  
HIROKI SUZUKI ◽  
...  

Direct numerical simulation (DNS) of turbulent planar jet with a second-order chemical reaction (A + B → R) is performed to investigate the processes of mixing and chemical reactions in spatially developing turbulent free shear flows. Reactant A is premixed into the jet flow, and reactant B is premixed into the ambient flow. DNS is performed at three different Damköhler numbers (Da = 0.1,1, and 10). Damköhler number is a ratio of a time scale of a flow to that of chemical reactions, and in this study, the large Da means a fast chemical reaction, and the small Da means a slow chemical reaction. The visualization of velocity field shows that the jet flow is developed by entraining the ambient fluid. The visualization of concentration of reactant A shows that concentration of reactant A for Da = 1 and 10 becomes very small in the downstream region because the chemical reaction consumes the reactants and reactant A is diffused with the jet development. By comparison of the profiles of chemical reaction rate and concentration of product R, it is found that product R for Da = 10 is produced by the chemical reaction at the interface between the jet and the ambient fluids and is diffused into the jet flow, whereas product R for Da = 0.1 is produced in the jet flow after reactants A and B are well mixed.


2020 ◽  
Vol 8 (37) ◽  
pp. 12800-12805
Author(s):  
Chengjia Xiong ◽  
Yangjie Lan ◽  
Bingda Chen ◽  
Zheng Li ◽  
Yu Zhang ◽  
...  

The extent of a chemical reaction and reaction rate are monitored according to the stopband shift curve of a photonic crystal with time.


1940 ◽  
Vol 13 (2) ◽  
pp. 255-261
Author(s):  
R. H. Gerke

Abstract One hundred years ago rubber was the only available substance having the property of long-range elasticity which makes rubber so useful to man. The invention of vulcanization tremendously increased the usefulness of rubber, since it decreased the plastic flow at elevated temperatures and increased the resistance to hardening at low temperatures. It is now the general consensus that vulcanization is caused by a chemical reaction or at least is attended by a chemical reaction. The fact that vulcanization is the result of a chemical reaction is an all-important factor in controlling the nature of the manufacturing processes in the rubber industry. The existence of a temperature coefficient of vulcanization like other chemical reactions exerts a powerful influence on the nature of the manufacturing processes. Thus, vulcanized rubber is made by a thermosetting rather than thermoplastic process.


Molecules ◽  
2021 ◽  
Vol 26 (3) ◽  
pp. 750
Author(s):  
Lu-Yan An ◽  
Zhen Dai ◽  
Bin Di ◽  
Li-Li Xu

It is counterintuitive that chemical reactions can be accelerated by freezing, but this amazing phenomenon was discovered as early as the 1960s. In frozen systems, the increase in reaction rate is caused by various mechanisms and the freeze concentration effect is the main reason for the observed acceleration. Some accelerated reactions have great application value in the chemistry synthesis and environmental fields; at the same time, certain reactions accelerated at low temperature during the storage of food, medicine, and biological products should cause concern. The study of reactions accelerated by freezing will overturn common sense and provide a new strategy for researchers in the chemistry field. In this review, we mainly introduce various mechanisms for accelerating reactions induced by freezing and summarize a variety of accelerated cryochemical reactions and their applications.


1981 ◽  
Vol 18 (01) ◽  
pp. 263-267 ◽  
Author(s):  
F. D. J. Dunstan ◽  
J. F. Reynolds

Earlier stochastic analyses of chemical reactions have provided formal solutions which are unsuitable for most purposes in that they are expressed in terms of complex algebraic functions. Normal approximations are derived here for solutions to a variety of reactions. Using these, it is possible to investigate the level at which the classical deterministic solutions become inadequate. This is important in fields such as radioimmunoassay.


1953 ◽  
Vol 26 (4) ◽  
pp. 902-911 ◽  
Author(s):  
C. S. Ramakrishnan ◽  
D. Raghunath ◽  
J. B. Pande

Abstract The chlorination of rubber solutions by gaseous chlorine was followed by isolating the partially chlorinated products and preparing their ozonides. The ozonides were hydrolyzed, and the acids and aldehydes formed on hydrolysis were determined. By a comparison with the amounts of acids and aldehydes obtained from ozonides of unreacted rubber, the amount of residual isoprenic double bonds present was found. The loss of double bonds attending the introduction of chlorine atoms into the molecule of rubber indicates four definite stages in chlorination : (1) initial substitutive attack by chlorine, with concomitant cyclization, resulting in a loss of one double bond between two isoprenic units, (2) substitution, (3) additive reaction, and (4) essentially substitution. Chlorination of aged rubber solutions differs from the above in that the cyclization reaction (stage 1) seems to be absent.


2012 ◽  
Vol 610-613 ◽  
pp. 1980-1985 ◽  
Author(s):  
Hong Jian Xu ◽  
Shu Fang Wang ◽  
Wei Guo Pan ◽  
Rui Tang Guo

The limestone-lime washing technology is the most widely used WFGD process, which normally we adopt to control the discharge of SO2 caused by coal’s combustion. Through the research on the oxidation kinetics of sulfite in this paper, it is indicated that macroscopic chemical reaction which responses to rate of sulfite is 1/2. And the results of orthogonal test can be concluded that: to the extent influence of oxidization reaction rate, the influences of temperature is the most significant, and influences of stirred speed is nearly negligible. The optimized operation factors may be shown as that temperature is controlled at 40°C, air ventilation is at 88ml/min,pH is 4.5 and stir speed is 500 r/min.


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