2016
DOI: 10.1016/j.vibspec.2016.03.013
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Regularity modes in Raman spectra of polyolefins: Part II. Polyethylene and ethylene copolymers

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Cited by 29 publications
(34 citation statements)
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“…As shown in the literature [47, 48, 50, 51], three Raman bands at 1,060, 1,080, and 1,130 cm −1 describing the C-C skeleton stretching vibrations of long-chain hydrocarbons are sensitive to the trans - gauche conformation order in lipids. The bands at 1,060 and 1,130 cm −1 appear in the Raman spectrum if the presence of trans-sequences is more than 6 and the length of a long alkyl chains contain more than 18 CH 2 groups, respectively [52, 53]. With a smaller number of CH 2 groups in the trans-sequence, the position of the Raman band at 1,130 cm −1 is shifted toward larger wavenumbers [53].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…As shown in the literature [47, 48, 50, 51], three Raman bands at 1,060, 1,080, and 1,130 cm −1 describing the C-C skeleton stretching vibrations of long-chain hydrocarbons are sensitive to the trans - gauche conformation order in lipids. The bands at 1,060 and 1,130 cm −1 appear in the Raman spectrum if the presence of trans-sequences is more than 6 and the length of a long alkyl chains contain more than 18 CH 2 groups, respectively [52, 53]. With a smaller number of CH 2 groups in the trans-sequence, the position of the Raman band at 1,130 cm −1 is shifted toward larger wavenumbers [53].…”
Section: Resultsmentioning
confidence: 99%
“…The bands at 1,060 and 1,130 cm −1 appear in the Raman spectrum if the presence of trans-sequences is more than 6 and the length of a long alkyl chains contain more than 18 CH 2 groups, respectively [52, 53]. With a smaller number of CH 2 groups in the trans-sequence, the position of the Raman band at 1,130 cm −1 is shifted toward larger wavenumbers [53]. Thus, Raman bands at 1,060 and 1,130 cm −1 characterize the lipid chains containing trans conformers (more ordered state), while the Raman band at 1,080 cm −1 characterizes the lipid chains containing only gauche conformers (less ordered state).…”
Section: Resultsmentioning
confidence: 99%
“…The bands at 2850 and 2883 cm À1 belong to the symmetric (n s (CH 2 )) and asymmetric (n as (CH 2 )) stretching vibrations of the CH 2 groups, respectively. 110,111 It is also possible to observe a weak The first is an overtone of wavenumbers in the range of 1400-1495 cm À1 (-CH 2 -bonds); the latter is reported to be the Fermi resonance between the CH 2 symmetric stretching and the overtone from the CH 2 bond. 123 Raman spectroscopy is sensitive to changes in the molecular structure level of PE, such as the degree of crystallinity, which is the key determining factor of PE density (i.e., higher the degree of crystallinity, higher the density).…”
Section: Band Assignment In the Raman Spectra Of Most Common Plastic Polymersmentioning
confidence: 98%
“…PE triggers only a few normal vibrations of infrared activity, due to its simple structure, high symmetry, and low polarity. Nevertheless, PE is extremely suitable for characterization using Raman spectroscopy because of its high activity and great peak intensity in Raman spectra . Figure presents the Raman spectra of SLL‐5 and GUR 4150.…”
Section: Resultsmentioning
confidence: 99%