Effect of Butyl Rubber Coating on Accelerated Aging of Natural Rubber

1986 ◽  
Vol 59 (1) ◽  
pp. 70-76 ◽  
Author(s):  
Bengt Stenberg ◽  
Lars-Olof Peterson ◽  
Per Flink ◽  
Folke Björk

Abstract From these results it is possible to draw the following conclusions: The primary protection against thermo-oxidative degradation comes from the butyl coating. The butyl coating works mainly by stopping diffusion of oxygen from the surrounding air, which is more important than stopping the antioxidant from diffusing out of the rubber, since the antioxidant effect is small.

2014 ◽  
Vol 87 (2) ◽  
pp. 370-382
Author(s):  
Jing Chen ◽  
Lanzhen He ◽  
Yasheng Chen ◽  
Jieping Zhong ◽  
Canzhong He ◽  
...  

ABSTRACT A novel model for calculating dehydrochlorination kinetics at a lower temperature of chlorinated natural rubber (CNR) is presented. It has been observed that dehydrochlorination is complex and involves three different stages. A model that accounts for dehydrochlorination at lower temperature is proposed. The kinetic parameters are obtained from dehydrochlorination experiments at 60–90 °C. The results of the kinetic calculation show that the apparent activation energy decreases with an increment of chlorine content. Higher chlorine content CNR makes it easier to remove hydrochloric acid when heated, but its dehydrochlorination rate affected by temperature is significantly less than that of the sample with a lower chlorine content. The thermogravimetric/derivative thermogravimetry results show that the beginning temperature of thermo-oxidative degradation rises with the increment of chlorine content. During the heating process, the higher chlorine content CNR is more stable than the lower one. The results suggest the storage conditions and basis for selection of appropriate temperature for the preparation of CNR from latex.


2014 ◽  
Vol 1004-1005 ◽  
pp. 245-248
Author(s):  
Chang Jin Yang ◽  
Yong Yue Luo ◽  
Bang Qian Chen ◽  
Kui Xu ◽  
Jie Ping Zhong ◽  
...  

Thermal and thermo-oxidative degradation of epoxidized natural rubber containing 25 mol % expoxidation (ENR25) with different four antioxidants were investigated by thermogravimetric analysis (TGA). The four antioxidants, viz., poly-2,2,4-trimethyl-1,2-dihydroqui- noline (RD), N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenedianine (4020), N-isopropyl-N'-phenyl- p-phenylenedi-amine (4010NA), and 2-mercaptobenzimidazole (MB) were used. The results indicate that the ENR25 vulcanizates with antioxidant 4020 or 4010NA is the optimal antioxidant for ENR25.


1978 ◽  
Vol 51 (1) ◽  
pp. 1-6 ◽  
Author(s):  
R. A. Pett ◽  
R. J. Tabar

Abstract For the type of natural rubber compound used in the impact absorbing bumper system, it has been shown that an apparent zero order reaction rate is valid for the degradation of tensile strength, elongation at break and tear strength during oven aging. The zero order rate applies to aging times beyond an induction period and prior to the onset of hardening. Since the rates follow the Arrhenius equation for rate-temperature dependence, accelerated aging can be readily applied to the prediction of long term changes in properties (within the temperature range of 82–171°C). The magnitude of the activation energy determined from losses in mechanical properties indicates the dominance of oxidative degradation as the mechanism of the losses in properties.


1958 ◽  
Vol 31 (4) ◽  
pp. 849-865 ◽  
Author(s):  
Jean le Bras ◽  
Jean-Claude Danjard ◽  
Madeleine Boucher

Abstract In order to better understand the complex phenomena related to aging, the two following propositions should be considered : (a) Each type of vulcanizate has a particular type of network structure, with characteristics dependent on the number and nature of the crosslinks between the macromolecules. Thermo-oxidative degradation may have varying effects according to the network points which are preferentially attacked. (b) The protection at present employed against the consequences of this degradation is based upon two different mechanisms, i.e., through the antioxidant effect, which retards the scission reaction, or through the deactivating effect, which helps to maintain the network by forming additional crosslinks. If we also take into account the fact that each accelerator is able, as is the deactivator, to create specific new bonds by after-cure, we may suggest an explanation for some unexplained aspects of the related phenomena. From our results and the derived deductions ideas emerge, from which it should be possible to establish, by logic (instead of empirically) and by adaptation to each type of vulcanizate, some rules for the best protection with the present-known protective agents. It should be noted that all preceding observations refer exclusively to the most widely used industrial practice, sulfur curing. However, the knowledge we now have of the deactivating effect mechanism has led us to think that it should also be possible, for vulcanizates produced with other vulcanizing agents, to find substances which will play the same part as our present deactivators, although of a totally different chemical composition. As a matter of fact, the so-called deactivators are but slow-acting crosslinking agents, the new crosslinks resulting from either a mobilization of the unused vulcanizing agent in the vulcanizate or from a direct intervention of the deactivator. We therefore doubt whether their name, derived from the first, and inexact, explanation given for their action, is still justified. However, to change it we should have to evoke an after-crosslinking, a source of confusion with other current terms ; moreover, a number of other wrong terms have been confirmed by use, for instance, the English “antioxidant”. As these deactivators make degradation less active, their original name is perhaps not so inappropriate after all.


2021 ◽  
Author(s):  
Zhen Zhang ◽  
Yuxin Zhang ◽  
Jiayi Li ◽  
Adeel Ahmad Hassan ◽  
Shifeng Wang

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