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Time‐resolved Raman spectroscopy of polystyrene under laser driven shock compression
Author(s) -
Rastogi Vinay,
Chaurasia S.,
Rao Usha,
Sijoy C. D.,
Mishra V.,
Kumar Manmohan,
Chaturvedi S.,
Deo M. N.
Publication year - 2017
Publication title -
journal of raman spectroscopy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.748
H-Index - 110
eISSN - 1097-4555
pISSN - 0377-0486
DOI - 10.1002/jrs.5166
Subject(s) - polystyrene , raman spectroscopy , shock (circulatory) , shock wave , laser , full width at half maximum , compression (physics) , materials science , molecular physics , bending , spectroscopy , analytical chemistry (journal) , wavenumber , optics , atomic physics , chemistry , physics , composite material , mechanics , optoelectronics , polymer , medicine , chromatography , quantum mechanics
The microscopic and dynamic response of the atactic polystyrene molecules under shock compression at laser power density of 4.9 GW/cm 2 was studied using time‐resolved Raman spectroscopy. The shock pressure estimated in the polystyrene sample was 2 GPa, and the temporal and wavenumber resolutions in these experiments were 3 ns and 3 cm −1 , respectively. The shocked polystyrene showed a blue shift of 5 and 7 cm −1 for the 1004 cm −1 (C―C―C ring bending mode ν 12 ) and 1606 cm −1 (C―C ring stretching mode ν 8 a . , respectively. The changes in ν 12 and ν 8 amodes are observed with respect to shock wave propagation. It is observed that the intensities of the Raman peaks decrease and the FWHM of the modes increase due to formation of additional new peaks with delay. The reason behind this indicates the mechanical processes associated with the uniaxial nature of the shock compression. The shock velocity inside the polystyrene was calculated as 2.9 ± 0.12 km/s using the evolution of intensity ratio of peaks with time. This is in good agreement with the shock velocity (3.0 km/s) deduced from the 2D simulations, performed using three temperature radiation hydrodynamic code, THRD. Copyright © 2017 John Wiley & Sons, Ltd.