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Spectroscopic Study of Di‐Imide Hydrogenation of Natural Rubber
Author(s) -
Samran Jareerat,
Phinyocheep Pranee,
Daniel Philippe,
Derouet Daniel,
Buzare JeanYves
Publication year - 2004
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.200451214
Subject(s) - degree of unsaturation , diimide , isomerization , olefin fiber , carbon 13 nmr , raman spectroscopy , natural rubber , double bond , chemistry , carbon black , materials science , polymer chemistry , organic chemistry , molecule , catalysis , physics , perylene , optics
The diimide hydrogenation of natural rubber (NR) was studied by using p ‐toluenesulfonylhydrazide (TSH) as a diimide‐releasing agent. The microstructure and the percentage of hydrogenation were studied by Raman, 1 H‐NMR and 13 C‐NMR spectroscopic techniques. Quantitative measurements on fraction of hydrogenated part gave the results in good agreement by using these techniques. The results indicated that percent hydrogenation increased with increasing of reaction time and about 80‐85 % hydrogenation was achieved when a two‐fold excess of TSH was used. The vibrational characteristic of C=C bond of NR is strongly Raman active and noted at 1663 cm −1 . The decrease of this signal was clearly observed during the progress of hydrogenation but the vibrational frequency of the cis and trans structures of the trisubstituted olefin unit of NR can not be differentiated by this technique. While 1 H‐ and 13 C‐NMR analysis showed that cis ‐ trans isomerization of carbon‐carbon unsaturation of NR occurred during hydrogenation.