Notes - Chain Scission in the Oxidation of Hevea. III. Effect of Temperature.

1956 ◽  
Vol 21 (3) ◽  
pp. 369-370 ◽  
Author(s):  
E. M. Bevilacqua
1956 ◽  
Vol 29 (4) ◽  
pp. 1274-1275
Author(s):  
E. M. Bevilacqua

Abstract When molecular oxygen reacts with raw Hevea rubber in latex at 90° C, two molecules of carbon dioxide and two molecules of “volatile acid” (one molecule of acetic acid and one molecule of formic acid) are produced for each apparent scission of the hydrocarbon chain, estimated from changes of solution viscosity. This corresponds to the complete destruction of one isoprene unit, and if the several hydrocarbon end groups are oxidized, requires a minimum of six molecules of oxygen per scission. Estimates of oxygen requirements for scission during the accelerated oxidation of vulcanized Hevea rubber much lower than this have been made. It has been suggested that the apparent high efficiency of scission in vulcanized rubber is the result of the predominance of scission at crosslinks over random cutting of the hydrocarbon chain. To investigate the less likely possibility that the mechanism of the reactions which leads to scission changes sharply with the rate of oxidation, the earlier estimates of yields of scissions and of volatile acids during the oxidation of Hevea latex at 90° C have been supplemented by measurements at 70° C and at 110° C.


1954 ◽  
Vol 27 (1) ◽  
pp. 120-133 ◽  
Author(s):  
J. Reid Shelton ◽  
Fred J. Wherley ◽  
William L. Cox

Abstract The same reaction appears to be rate-controlling in the oxidation of natural rubber and GR-S stocks at all temperatures in the range studied, 50° to 110° C. This is apparent from the linear relationship established between rate of oxygen absorption and the reciprocal of the absolute temperature. Presumably this would also be true for a reasonable extrapolation to lower or higher temperatures. Thus it is possible to determine the probable rate of oxygen absorption at room temperature on the basis of data obtained in short-term tests at higher temperatures, provided data are available at several temperatures. The effect on properties which accompanies the absorption of a given amount of oxygen varies with the temperature. For example, aging at higher temperatures produces a softer stock with lower modulus and higher elongation than is obtained by the absorption of the same amount of oxygen at a lower temperature. Thus chain scission predominates at higher temperatures, while cross-linking becomes of greater relative importance at lower temperatures. These facts, together with the observation that the same reaction is rate-controlling at all temperatures studied, indicate that the degradation reactions must be secondary reactions which are not rate-controlling. One cannot predict the aging characteristics of a stock by the use of an accelerated test at only one temperature. It is possible, however, to establish a quantitative measure of the rate of change in a given property (per unit amount of oxygen absorbed) as a function of temperature by means of tests at more than one temperature. Thus it is now possible to utilize short-term oxygen-absorption measurements at, say, three temperatures to establish the relationships, and then to extrapolate the data to lower temperatures and predict the time required to absorb a given amount of oxygen and the degradation of properties to be expected under comparable conditions at the lower temperature. If a change from oxygen to air is also involved, the effect of the changes in oxygen concentration must also be taken into account.


Author(s):  
P. R. Swann ◽  
W. R. Duff ◽  
R. M. Fisher

Recently we have investigated the phase equilibria and antiphase domain structures of Fe-Al alloys containing from 18 to 50 at.% Al by transmission electron microscopy and Mössbauer techniques. This study has revealed that none of the published phase diagrams are correct, although the one proposed by Rimlinger agrees most closely with our results to be published separately. In this paper observations by transmission electron microscopy relating to the nucleation of disorder in Fe-24% Al will be described. Figure 1 shows the structure after heating this alloy to 776.6°C and quenching. The white areas are B2 micro-domains corresponding to regions of disorder which form at the annealing temperature and re-order during the quench. By examining specimens heated in a temperature gradient of 2°C/cm it is possible to determine the effect of temperature on the disordering reaction very precisely. It was found that disorder begins at existing antiphase domain boundaries but that at a slightly higher temperature (1°C) it also occurs by homogeneous nucleation within the domains. A small (∼ .01°C) further increase in temperature caused these micro-domains to completely fill the specimen.


Author(s):  
T. Geipel ◽  
W. Mader ◽  
P. Pirouz

Temperature affects both elastic and inelastic scattering of electrons in a crystal. The Debye-Waller factor, B, describes the influence of temperature on the elastic scattering of electrons, whereas the imaginary part of the (complex) atomic form factor, fc = fr + ifi, describes the influence of temperature on the inelastic scattering of electrons (i.e. absorption). In HRTEM simulations, two possible ways to include absorption are: (i) an approximate method in which absorption is described by a phenomenological constant, μ, i.e. fi; - μfr, with the real part of the atomic form factor, fr, obtained from Hartree-Fock calculations, (ii) a more accurate method in which the absorptive components, fi of the atomic form factor are explicitly calculated. In this contribution, the inclusion of both the Debye-Waller factor and absorption on HRTEM images of a (Oll)-oriented GaAs crystal are presented (using the EMS software.Fig. 1 shows the the amplitudes and phases of the dominant 111 beams as a function of the specimen thickness, t, for the cases when μ = 0 (i.e. no absorption, solid line) and μ = 0.1 (with absorption, dashed line).


1990 ◽  
Vol 80 (3) ◽  
pp. 431-436 ◽  
Author(s):  
Isabelle Delvallee ◽  
Annie Paffen ◽  
Geert-Jan De Klerk

1973 ◽  
Vol 29 (01) ◽  
pp. 183-189
Author(s):  
C. A Praga ◽  
E. M Pogliani

SummaryTemperature represents a very important variable in ADP-induced platelet aggregation.When low doses of ADP ( < 1 (μM) are used to induce platelet aggregation, the length of the incubation period of PRP in the cuvette holder of the aggregometer, thermostatted at 37° C, is very critical. Samples of the same PRP previously kept at room temperature, were incubated for increasing periods of time in the cuvette of the aggregometer before adding ADP, and a significant decrease of aggregation, proportional to the length of incubation, was observed. Stirring of the PRP during the incubation period made these changes more evident.To measure the exact temperature of the PRP during incubation in the aggre- gometer, a thermocouple device was used. While the temperature of the cuvette holder was stable at 37° C, the PRP temperature itself increased exponentially, taking about ten minutes from the beginning of the incubation to reach the value of 37° C. The above results have a practical significance in the reproducibility of the platelet aggregation test in vitro and acquire particular value when the effect of inhibitors of ADP induced platelet aggregation is studied.Experiments carried out with three anti-aggregating agents (acetyl salicyclic acid, dipyridamole and metergoline) have shown that the incubation conditions which influence both the effect of the drugs on platelets and the ADP breakdown in plasma must be strictly controlled.


1967 ◽  
Vol 17 (01/02) ◽  
pp. 112-119 ◽  
Author(s):  
L Dintenfass ◽  
M. C Rozenberg

SummaryA study of blood coagulation was carried out by observing changes in the blood viscosity of blood coagulating in the cone-in-cone viscometer. The clots were investigated by microscopic techniques.Immediately after blood is obtained by venepuncture, viscosity of blood remains constant for a certain “latent” period. The duration of this period depends not only on the intrinsic properties of the blood sample, but also on temperature and rate of shear used during blood storage. An increase of temperature decreases the clotting time ; also, an increase in the rate of shear decreases the clotting time.It is confirmed that morphological changes take place in blood coagula as a function of the velocity gradient at which such coagulation takes place. There is a progressive change from the red clot to white thrombus as the rates of shear increase. Aggregation of platelets increases as the rate of shear increases.This pattern is maintained with changes of temperature, although aggregation of platelets appears to be increased at elevated temperatures.Intravenously added heparin affects the clotting time and the aggregation of platelets in in vitro coagulation.


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