An Infrared Spectrometric Study of the Oxidation of Natural Rubber

1952 ◽  
Vol 25 (2) ◽  
pp. 251-257
Author(s):  
L. D'Or ◽  
I. Kössler

Abstract The kinetics of the oxidation of natural rubber by atmospheric oxygen has been studied by various methods, for example, by volumetric and manometric measurements of the absorption of oxygen, by measurements of the increase of weight of the rubber, and by changes in the mechanical properties as a function of time. However, the oxidation of rubber is a complex phenomenon, and none of these techniques offers a means of following the oxidation in detail. In principle, it is possible, by infrared absorption spectrometry, to detect the presence of different groups which are present in a given sample of rubber and to determine their concentrations. Hence, it was hoped that this technique would offer a means of studying the various phenomena involved in the oxidation of rubber. In fact, this technique has already been employed in studies of the structure of rubber as well as in the qualitative and quantitative analysis of synthetic products. In addition to these already published studies, various authors have reported that the oxidation of natural rubber results in changes in its infrared spectrum, but none of the investigators has followed these changes quantitatively. Nevertheless, the possible interest of such a quantitative study, when carried out in parallel with a study of the changes in mechanical properties, has been pointed out by different authors. The authors of the present work decided, as a first approach to the problem, to prepare samples of rubber which could be studied by infrared absorption. The progress of oxidation could then be followed quantitatively by the disappearance of the principal groups present in rubber which had not undergone oxidation and the formation of characteristic groups in the oxidation products. Finally, from the data obtained, it was hoped, if not to draw conclusions as to the mechanism or mechanisms of oxidation, at least to obtain some indications of the precise kinetics of this oxidation.

2000 ◽  
Vol 627 ◽  
Author(s):  
Nathalie Sommier ◽  
Patrice Porion ◽  
Pierre Evesque

ABSTRACTMagnetic Resonance Imaging (MRI) technique was used to study the mixing and segregation processes of granular materials in a sophisticated tumbling blender (Turbula® mixer) using binary mixtures of sugar beads of different diameters d. Its motion generates mixtures with complex patterns. Effects of some parameters (beads diameter ratio, rotation speed, mixing time) were checked on segregation and mixing processes. We report in this paper, a qualitative and quantitative analysis of these phenomena. A segregation index S was defined to study the homogeneity and the kinetics of the mixing/segregation processes. When the ratio of bead diameters dmax/dmin is approximately 1, mixing process is observed but segregation occurs as soon as dmax/dmin is greater than 1.1.


2012 ◽  
Vol 28 (4) ◽  
pp. 201-220 ◽  
Author(s):  
Rejitha Rajan ◽  
Siby Varghese ◽  
K.E. George

This study was undertaken to optimize the vulcanization conditions and explore the effect of residual peroxide in the peroxide vulcanization of natural rubber. The study was followed through the kinetics of the vulcanization reaction at various temperatures viz. 150,155,160 and 165°C. Dicumyl peroxide (DCP) was used as the crosslinking agent. The Monsanto Rheometer was used to investigate the different crosslinking stages and vulcanization kinetics. The thermal decomposition of peroxide followed a first order free radical decomposition reaction. Half-lives at various temperatures were determined. The percentage of residual peroxide was calculated from the cure kinetic data. The effect of residual peroxide on mechanical properties was studied at various peroxide levels and also by extending the cure time (from t90 to t95 and then to t100). Mechanical properties such as tensile strength, elongation at break, modulus and compression set (70 and 100°C) were measured. Excess peroxide was found to cause a high compression set at elevated temperature and the cure time was selected to achieve minimum residual peroxide in the product. Results indicate that peroxide concentration is the dominant factor controlling the crosslink density and hence the properties of the vulcanizates.


2020 ◽  
Vol 305 ◽  
pp. 00006
Author(s):  
Niculina-Sonia Şuvar ◽  
Maria Prodan ◽  
Irina Vasilica Nălboc ◽  
Andrei Szollosi-Moţa

The transitions between the vibrational energetic states of atoms represent the infrared absorption spectra, which is a band spectrum over which the transitions between energetic rotational states overlap. One of the most important uses of infrared absorption spectrometry is the identification in quantitative terms of the structure of compounds from a substance, the analytes being either solid, liquid or vaporous. The FTIR-TGA Coupling is a technique that permanently controls the mass loss in a sample, as a function of temperature and time, as well as the identification and recording of various compounds occurring during the combustion process. Research on hydraulic oils has consisted of their analysis using the FTIR-TGA coupling in order to identify flammable substances that can generate explosive events.


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