Production of 1,3-propanediol via in situ glycerol hydrogenolysis in aqueous phase reforming using bimetallic W-Ni/CeO 2

• Published in: Environmental science and pollution research international 2024-10
• Main Authors: Md Radzi, Mohamad Razlan, Rosli, Siti Nor Amira, Yusoff, Mohd Hizami Mohd, Abidin, Sumaiya Zainal
• Format: Article
• Language: English
• ISSN: 1614-7499
• DOI: 10.1007/s11356-024-35262-x

The production of 1,3-propanediol via in situ glycerol hydrogenolysis and aqueous phase reforming is a promising technique to ensure high product yield with shorter reaction times and lower costs, as demonstrated in this study by investigating the effect of tungsten (W) doping on Ni/CeO catalysts. Physicochemical properties of catalyst were determined using XRD, H -TPR, NH -TPD, BET, and FESEM-EDX techniques, and the catalytic performance was investigated at 230 °C, 20 bar, and 5 wt.% glycerol in an autoclave batch reactor. W doping ranging from 1-7% improved the catalyst's performance, with 3% W in 10% Ni/CeO₂ (3W10NC) achieving the highest yield (2.4%), selectivity (33.3%), and a good conversion rate (72.18%). The effect of reaction parameter on the 3W10NC catalyst showed that increasing pressure and temperature from the initial parameters had a detrimental effect on 1,3-propanediol attributed to the phenomenon called over-hydrogenolysis. Increasing the glycerol concentration to 20 wt.% also had a positive effect, resulting in the highest 1,3-propanediol yield of 22.27%. The effect of reaction time study revealed that the yield of 1,3-propanediol continued to increase steadily, reaching 38.29% after 4 h of reaction under the optimal conditions of 230 °C, 20 bar, and 20 wt.% glycerol. The kinetic study confirmed that the reaction follows first-order reaction with activation energy of 20.104 kJ mol . The catalyst reusability test revealed a decrease in the yield of 1,3-propanediol to 32.55%, likely due to deactivation caused by sintering and leaching, as indicated by the FESEM micrograph, EDX spectra, and NH -TPD.