The Degree of Crystallinity in Natural Rubber. IV. The Degree of Crystallization in Frozen Raw Rubber and Stretched Vulcanized Rubber

1950 ◽  
Vol 23 (2) ◽  
pp. 310-319 ◽  
Author(s):  
J. M. Goppel ◽  
J. J. Arlman

Abstract An improved x-ray technique has been worked out to determine the degree of crystallinity in natural rubber. Inaccuracies which sometimes occur in quantitative x-ray measurements were eliminated, and it has been shown that the amount of crystalline rubber, both in frozen samples of raw rubber and in stretched vulcanized rubber, could be determined fairly accurately. More experiments were carried out and the results are described. These results, which confirm the current views on the problem of crystallization, point to relatively low degress of crystallization, even in highly stretched rubber, and they agree with some other experimental evidence and with a recent theoretical investigation.

1950 ◽  
Vol 23 (2) ◽  
pp. 306-310 ◽  
Author(s):  
J. J. Arlman

Abstract In 1925 Katz discovered the crystallization of stretched rubber. In the following years several investigators tried to determine the structure of rubber crystallites. The densities of the rubber crystallites calculated from the results of these investigations varied strongly. The results of x-ray and density measurements on crude rubber carried out by the author can be made to correspond only when the latter are based on the unit cell of Bunn. It is shown by experiment that, to measure the correct degree of crystallization, it is necessary to use monochromatic x-rays.


1950 ◽  
Vol 23 (2) ◽  
pp. 319-325 ◽  
Author(s):  
J. J. Arlman ◽  
J. M. Goppel

Abstract A recent theory, developed by Flory, makes it possible to calculate the degree of crystallization from thermodynamical measurements if certain parameters are properly evaluated. Such evaluation is possible by combining Wildschut's thermodynamical measurements with the x-ray results presented in previous papers. Thus the average length of molecule chains between cross-linkages can be derived; it closely corresponds to the results of swelling measurements carried out by Gee. Other parameters are also evaluated in agreement with their physical meaning.


1948 ◽  
Vol 21 (4) ◽  
pp. 773-783 ◽  
Author(s):  
J. M. Goppel

Abstract There are indications that the degree of crystallization in high polymeric substances is of importance in studying mechanical properties. With regard to the crystallization of rubber, few measurements have been made, mainly by Field. The results, however, are in contradiction to estimates of an earlier date, and therefore the necessity was felt to have them checked. An x-ray method, in some respecta differing from that of Field, was developed, the results of which diverged considerably from the figures reported by Field. The present article deals with a description of the method.


1951 ◽  
Vol 24 (4) ◽  
pp. 845-852
Author(s):  
B. B. S. T. Boonstra

Abstract To elucidate the crystallization phenomenon in natural rubber and to investigate the applicability of thermodynamic calculation to measurements of the elastic tension as a function of temperature, it seemed necessary to check whether crystallization determined by x-ray analysis (and combined with density) lined up reasonably with the percentage of crystallization computed from the energy change found by applying thermodynamics to stretched vulcanized rubber) on stretching. Calorimetric measurements were desirable, as no accurate figures are available for the heat of crystallization of rubber crystallites. The heat of melting of rubber crystallites was determined to about 66 joules per gram, which is of the same order as that of isoprene. The spreading in the results was large; the determination is based on the degree of crystallization found by x-ray analysis of raw rubber. The heat of crystallization on stretching, found by thermodynamic evaluation of the elastic tension and its temperature coefficient, is combined with the value of 66 joules for the heat of melting of the pure rubber crystallites. The degree of crystallization calculated in this way agrees reasonably well with the direct x-ray measurements of Goppel and Arlman. Crystallization as determined by x-ray analysis and that responsible for the energy change on stretching are much the same. This also means that thermodynamic evaluation of the change of stress with temperature is justified if pufficient relaxation of stress has taken place.


1948 ◽  
Vol 21 (4) ◽  
pp. 783-789
Author(s):  
J. M. Goppel

Abstract In the foregoing article a method for determining the proportion of crystalline rubber in stretched samples has been described. A complication due to varying crystallite orientation in different samples appeared to interfere with the application. A simple relation is given between the degree of orientation and an empirical constant which makes possible a rapid determination of the degree of crystallization, regardless of the orientation in the sample under investigation.


2021 ◽  
Vol 285 ◽  
pp. 07034
Author(s):  
Yulia Tertyshnaya ◽  
Maksim Zakharov ◽  
Alina Ivanitskikh ◽  
Anatoliy Popov

In the work an eco-friendly non-woven fiber made of polylactide and natural rubber with a rubber content from 0 to 15 wt.% was obtained by electrospinning. The influence of distilled water and UV irradiation on the agrofibers has been investigated. The water sorption test showed that the addition of natural rubber into the polylactide matrix does not significantly affect the degree of water absorption of the fibrous materials, which is in the range of 49-50.6%. Thermal characteristics after 180 days of degradation in distilled water at 22±2 oC and UV irradiation at a wavelength of 365 nm during 100 hours were determined using the differential scanning calorimetry. Changes in the values for glass transition and melting temperatures, and the degree of crystallinity were determined.


Polymers ◽  
2021 ◽  
Vol 13 (20) ◽  
pp. 3536
Author(s):  
Indra Surya ◽  
Kamaruddin Waesateh ◽  
Abdulhakim Masa ◽  
Nabil Hayeemasae

Halloysite Nanotubes (HNT) are chemically similar to clay, which makes them incompatible with non-polar rubbers such as natural rubber (NR). Modification of NR into a polar rubber is of interest. In this work, Epoxidized Natural Rubber (ENR) was prepared in order to obtain a composite that could assure filler–matrix compatibility. However, the performance of this composite was still not satisfactory, so an alternative to the basic HNT filler was pursued. The surface area of HNT was further increased by etching with acid; the specific surface increased with treatment time. The FTIR spectra confirmed selective etching on the Al–OH surface of HNT with reduction in peak intensity in the regions 3750–3600 cm−1 and 825–725 cm−1, indicating decrease in Al–OH structures. The use of acid-treated HNT improved modulus, tensile strength, and tear strength of the filled composites. This was attributed to the filler–matrix interactions of acid-treated HNT with ENR. Further evidence was found from the Payne effect being reduced to 44.2% through acid treatment of the filler. As for the strain-induced crystallization (SIC) in the composites, the stress–strain curves correlated well with the degree of crystallinity observed from synchrotron wide-angle X-ray scattering.


2007 ◽  
Vol 29-30 ◽  
pp. 337-340 ◽  
Author(s):  
M.A. Sawpan ◽  
K.L. Pickering ◽  
Alan Fernyhough

The potential of hemp fibre as a reinforcing material for Poly(lactic acid) (PLA) was investigated. Good interaction between hemp fibre and PLA resulted in increases of 100% for Young’s modulus and 30% for tensile strength of composites containing 30 wt% fibre. Different predictive ‘rule of mixtures’ models (e.g. Parallel, Series and Hirsch) were assessed regarding the dependence of tensile properties on fibre loading. Limited agreement with models was observed. Differential scanning calorimetry (DSC) and x-ray diffraction (XRD) studies showed that hemp fibre increased the degree of crystallinity in PLA composites.


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