THE THERMAL DECOMPOSITION OF OZONE. III. THE TEMPERATURE COEFFICIENT OF REACTION RATE

1927 ◽  
Vol 49 (7) ◽  
pp. 1650-1664 ◽  
Author(s):  
Oliver R. Wulf ◽  
Richard C. Tolman
2019 ◽  
Author(s):  
Milad Narimani ◽  
Gabriel da Silva

Glyphosate (GP) is a widely used herbicide worldwide, yet accumulation of GP and its main byproduct, aminomethylphosphonic acid (AMPA), in soil and water has raised concerns about its potential effects to human health. Thermal treatment processes are one option for decontaminating material containing GP and AMPA, yet the thermal decomposition chemistry of these compounds remains poorly understood. Here, we have revealed the thermal decomposition mechanism of GP and AMPA by applying computational chemistry and reaction rate theory methods. <br>


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.


1972 ◽  
Vol 50 (11) ◽  
pp. 1743-1750 ◽  
Author(s):  
G. K. Diedrich ◽  
P. Kruus ◽  
L. M. Rachlis

The formation of polymers has been observed on exposure of pure substituted benzenes to ultrasound intense enough to cause cavitation. The products have some of the characteristics of the char obtained from low temperature pyrolysis of hydrocarbons. They are difficult to dissolve, melt above 300 °C, and give a large broad e.p.r. signal. A crude correlation between bond dissociation energy and the reaction rate suggests that the initiation reaction is a thermal decomposition in a cavitation bubble. The phenomenon is compared to radiolysis and thermal reactions.


Author(s):  
Saddam Al-Hammadi ◽  
Gabriel da Silva

We have studied the decomposition and isomerization of furfural in the gas-phase using quantum chemical and statistical reaction rate theory techniques. This work uncovers a variety of new reaction channels...


Steacie and Shaw have made a study of the thermal decomposition of a series of alkyl nitrites at temperatures between 170° and 240°. Their results are contained in the series of papers to which reference is made; but of these only the first is at present significant, for in it they consider the decomposition of methyl nitrite, and give their reasons for the conclusions which they arrive at regarding the nature of the decomposition process, which they assume to be common to the whole series. Their results led them to the conclusion that the decomposition process proceeds in accordance with the equation, 2CH 3 NO 2 = CH 2 O + CH 4 O + 2NO, (1) the process being of the first order. Assuming that this was so, the critical increment calculated from the temperature coefficient was found to be 36⋅4 kcals. If the decomposition process really does take place in accordance with the equation written above, the conclusion that the process is uni-molecular is confusing rather than helpful. It appeared possible that a study of the problem by methods more detailed than that applied by Steacie and Shaw might throw further light upon it, and with that object in view the present work was undertaken.


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