Table 1 The FT-IR analysis was done to identify different organic species present in the aqueous product, collected from the microreactor operating at 2.5–3.0 V.
Assigned Peak no. in Fig. 4 | Peak position in Fig. 4 (cm−1) | Assigned functional groups | Classification of the Organic compounds likely to present as end product42 | Vibration mode | Typical vibrational frequency range (cm−1)42 | Peak intensity |
---|---|---|---|---|---|---|
1 | 3454 | O–H | Dimeric Alcohols/phenols | Stretching | 3584–3230 | Strong |
2 | 2922 | –CH2– | Alkane | Stretching | 2924–2859 | Strong |
3 | 2859 | –O–CH3 | Ether | Stretching | 2924–2859 | Strong |
4 | 2859 | –CHO | Aldehydes | Stretching | 2924–2859 | Strong |
5 | 2361 | C=NH+ | NH+ Charged amines | Stretching | 2500–2325 | Weak |
6 | 1632 | C=C | Non-conjugated Alkene | Stretching | 1635 | Strong |
7 | 1401 | C–H | Esters | Bending | 1430–1400 | Weak |
8 | 1314 | C–OH | Primary alcohols | Stretching | 1350–1260 | Weak |
9 | 1257 | C–O | Esters of aromatic acids | Stretching | 1300–1250 | Weak |
10 | 1181 | C–O | Higher Esters | Stretching | 1200–1170 | Weak |
11 | 1100 | C–OH | Secondary alcohols | Stretching | 1120–1100 | Weak |