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Characterization of ethylene in EP and in iPP/EP systems by deconvolution of IR spectra

✍ Scribed by D. Daoust; S. Bebelman; N. Chaupart; R. Legras; J. Devaux; J. Costa


Book ID
101253493
Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
186 KB
Volume
75
Category
Article
ISSN
0021-8995

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✦ Synopsis


The purpose of this study is to propose a correlation between IR spectra and molecular structure of ethylene-propylene (EP) copolymers possibly blended with isotactic polypropylene (iPP). The method is based on the deconvolution of the spectrum in the CH 2 -rocking range, i.e., 800 -680 cm Οͺ1 , where the bands of interest overlap. The six bands present in this region were signal averaged in position and width. The spectra were then deconvoluted (curve fitted) assuming a Lorentzian shape for the bands. The band at 1167 cm Οͺ1 (with a shoulder at 1156 cm Οͺ1 ) corresponding to a CH 3 vibration is considered as an internal standard. The method was checked by varying some fitting parameters. In order to realize some quantitative measurements, calibration curves were established with some EP samples, characterized by 13 C NMR, which were used as standards. The amounts of total O(CH 2 OCH 2 )O units (ethylene units), isolated ethylene and structural defaults in PP were determined for different iPP/EP blends. Ethylene crystallinity has also been determined. A good correlation was evidenced between infrared and 13 C NMR measurements.


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NMR, differential scanning calorimetry,
✍ F. LauprΓͺtre; S. Bebelman; D. Daoust; J. Devaux; R. Legras; J. L. Costa πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 224 KB πŸ‘ 2 views

High-resolution solid-state 13 C-NMR, differential scanning calorimetry, and Fourier transform infrared spectroscopy were used to compare the very low crystalline degree and crystallite dimensions of ethylene runs in a series of isotactic polypropylene/ethylene-propylene copolymer blends exhibiting