Table 3.
Run | Peak | Trans. | Assignment |
---|---|---|---|
1 | 3582.74 | 86.21 | O–H stretching vibration |
2 | 3122.40 | 25.73 | C–H symmetric stretching vibration of the connection of the in CH2 group |
3 | 2598.51 | 36.05 | C–H stretching vibration, of aliphatic Alkane |
4 | 2496.73 | 57.11 | O–H stretching vibration |
5 | 2296.43 | 80.26 | CH3 group stretching vibrations |
6 | 1750.64 | 84.37 | C=O stretching vibration of a carbonyl bond |
7 | 1398.41 | 85.72 | CH3 symmetric bending vibrations |
8 | 1200.08 | 72.14 | C–O–C asymmetric stretching vibration |
9 | 1126.28 | 81.92 | C–O–C and C–C–O Stretching vibration due to the accumulation of polyester compounds (poly-3-hydroxybutyrate and probably phospholipids (PLs)) |
10 | 1000.73 | 52.17 | C–O–C and C–C–O Stretching vibration due to the accumulation of polyester compounds (poly-3-hydroxybutyrate and probably phospholipids (PLs)) |
11 | 984.15 | 20.00 | C–C–O stretching vibration |
12 | 862.40 | 64.38 | C–O Stretching vibration |
13 | 800.24 | 84.49 | CH bending vibration |
14 | 700.06 | 76.82 | Rocking CH2 mode due to the accumulation of polyesters |
15 | 550.31 | 92.71 | C–Cl C–Br, I Stretching vibrations |
Trans. represent transmittance (%). Peak is cm−1