Catalyst | Synthesis Method | Test Parameters | Observations | H2 % | Ref. | |
Achievements | Limitations | |||||
Co & La supported Zn, Al-Htlc | Co-precipitation followed by calcination at 600˚C for 3 h | 400˚C - 600˚C & atmospheric pressure | Better EtOH conversion, high H2 selectivity, and good catalyst stability | EtOH conversion decreased at a lower temperature | 75.1 | [32] |
NiCo-MgAl mixed oxide prepared from Htlc | Ultrasound or microwave radiation assisted co-precipitation followed by thermal decomposition at 500˚C for 16 h | 550˚C | Ultrasound or microwave treatment reduced catalyst synthesis time and increased reducibility and basicity of the catalyst | Increase in basicity decreased H2 yield due to the formation of unwanted byproducts | 77 | [141] |
Co-Mg-Al | Ultrasound-assisted co-precipitation followed by calcination at 600˚C for 8 h | 600˚C & atmospheric pressure | Catalysts with 10% to 15% Co exhibited the best hydrogen yield due to good dispersion of active phase, large surface area and non-agglomeration of the catalyst | Co concentrations less than 10% promotes unwanted product formation and rapid catalyst deactivation | - | [142] |
K doped Co/Mg/Al-Htlc | Co-precipitation for Htlc precursor and wet impregnation for K doping followed by calcination at 550˚C for 4 h | 400-600˚C & 1 - 18 bar pressure | K doped Co-Htlc catalyst exhibited good stability and no C accumulation happened during the catalytic operation | Staged membrane reactor exhibited lower H2 yields because of the H2 removal from the reaction medium | 80 | [143] |
Ni-Mg/Al-Htlc | Co-precipitation and then calcination for 4 h at 500˚C in air | 200˚C - 650˚C | In dilute condition (3% EtOH) catalyst reduced at 450˚C with H2 provided completeEtOH conversion and CO free H2 production | At higher temperatures, ethanol conversion decreased and amount of CO in the product stream increased | 76 | [144] |
Shell core La-Ni(Mg-AL)O3 at Mg-Al | Co-precipitation followed by calcination at 700˚C - 900˚C for 6 h | 700˚C & Atmospheric pressure | The developed shell-core catalyst at temperature ≥ 700˚C showed good stability and high activity during EtOH steam reforming | Catalyst calcined at high temperature (900˚C) caused the spinel phase and coke formation during the reaction | 4.0 mol/mol Et-OH | [145] |