Results of catalyst screening for selective hydroconversion of dodecanoic acid into dodecane-1-ol.
Entry | Catalysta | Conversionb (%) | Yieldb(%) | ||
---|---|---|---|---|---|
Dodecane-1-ol | n-Dodecane | Othersc | |||
1 | Ru/TiO2 | 73 | 65 | 4 | 4 |
2 | Ru–(0.026)MoOx/TiO2(A) | >99 | 61 | 38 | Trace |
3 | Ru–(0.026)MoOx/TiO2(R) | >99 | 82 | 10 | 8 |
4d | Ru/TiO2 + (NH4)6Mo7O24·4H2O | >99 | 45 | 9 | 46 |
5d | Ru/TiO2 + MoOx | 97 | 42 | 12 | 43 |
6e | Ru@MoOx | 98 | 59 | 7 | 32 |
The amount of Mo was arround 0.025 mmol (1 wt% to Ru metal based on the amount of precursor). Reaction conditions: catalyst, 0.065 g; lauric acid, 3.2 mmol; solvent, 2-propanol: H2O, 5 ml (4.0 : 1.0 volume ratio), 170 °C; H2 40 bar, 7 h.
Conversion and yield were determined by GC using an internal standard technique.
Others include dodecyl dodecanoate as the esterification of lauric acid and dodecane-1-ol and products with smaller carbon number according to GC-MS profiles.
The catalysts were prepared using physical mixing at room temperature, dried at 110 °C for 5 h, followed by reduction with H2 at 500 °C for 3 h.
The catalyst was prepared using one-pot hydrothermal of RuCl3 and (NH4)6Mo7O24·4H2O mixture solutions at 150 °C for 24 h, followed by reduction with H2 at 500 °C for 3 h. The carbon balance was 93–96% for all the catalyst.