Table 6.
Run | Peak | Trans | Assignment |
---|---|---|---|
1 | 3998.26 | 56.19 | O–H stretching vibration |
2 | 3308.41 | 22.84 | Strong N–H stretching vibration of H-bonding (due to water) and possible metal binding of amide groups in proteins |
3 | 3199.74 | 14.94 | C–H stretching vibration, of aliphatic Alkane |
4 | 3021.58 | 32.71 | C–H symmetric stretching vibration of the connection of the in CH2 group |
5 | 2999.58 | 36.28 | C–H symmetric stretching vibration of the connection of the in CH2 group |
6 | 2982.55 | 38.49 | C–H stretching vibration |
7 | 2843.62 | 43.21 | RCH = N=N stretching vibration |
8 | 2228.71 | 52.70 | C≡N stretching vibrations |
9 | 1400.97 | 28.15 | CH2 symmetric bending vibration |
10 | 1200.04 | 31.57 | C–O–C asymmetric stretching vibration |
11 | 1026.48 | 32.20 | C–O–C and C–C–O Stretching vibration due to the accumulation of polyester compounds (poly-3-hydroxybutyrate and probably phospholipids (PLs)) |
12 | 898.27 | 52.10 | C–C Stretching vibration of amide group |
13 | 800.00 | 48.76 | CH bending vibration of alkenes |
14 | 747.35 | 48.75 | Rocking CH2 mode due to the accumulation of polyesters |
15 | 632.07 | 46.21 | C–O Stretching vibration |
16 | 530.73 | 38.94 | C–Cl C–Br, I Stretching vibrations |
Trans. represent transmittance (%). Peak is cm−1