The aqueous phase reforming (APR) of glycerol was studied using sonochemically synthesized 10%Ni-x%Ca/ZrO2 catalysts (where x = 0, 0.5, 3, and 5) for the production of value-added liquid products. The APR reaction was performed in a batch reactor under the following conditions: 20 bar, 230 °C 450 rpm, and 1 h of reaction time. The synthesized catalysts were characterized using XRD, FESEM, BET, and H2-TPR to observe the effect of Ca doping on the physio-chemical properties of the catalysts. The results revealed that, at higher Ca loading, the catalysts experienced serious particles’ agglomeration, which resulted in a larger particles’ size, smaller surface area, and smaller pore volume owing to uneven distribution of the particles. The characterization results of the catalysts confirmed that the Us catalysts have a slightly higher surface area, pore volume, and pore size, as well as highly reducible and fine crystalline structure, compared with WI catalysts. The catalytic performance of the catalysts shows that 1,3-propanediol (1,3-PDO) and 1,2-propanediol (1,2-PDO) were the two main liquid products produced from this reaction. The highest selectivity of 1,3-PDO (23.84%) was obtained over the 10%Ni/ZrO2 catalyst, while the highest selectivity of 1,2-PDO (25.87%) was obtained over the 10%Ni-5%Ca/ZrO2 catalyst.
The catalytic steam reforming of oxygenated hydrocarbons has been holding an interest in scientific societies for the past two decades. The hydrogen production from steam reforming of glycerol, ethanol and other oxygenates such as ethylene glycol and propylene glycol are more suitable choice not just because it can be produced from renewable sources, but it also helps to decrease the transportation fuel price and making it more competitive. In addition, hydrogen itself is a green fuel for the transportation sector. The studies on the production of hydrogen from various reforming technologies revealed a remarkable impact on the environmental and socio-economic issues. Researchers became more focused on glycerol steam reforming (GSR), ethanol steam reforming (ESR) and other oxygenates to investigate the catalyst suitability, their kinetics and challenges for the sustainability of the oil and gas production. In the present work, the authors critically addressed the challenges and strategies for hydrogen production via GSR, ESR and other oxygenates reforming process. This review covers extensively thermodynamic parametric analysis, catalysts developments, kinetics and advancement in the operational process for glycerol, ethanol and few other oxygenates. This detailed investigation only highlights the steam reforming process (SRP) of these oxygenates at the laboratory experimental stage. It was found that from this review, there are many technical issues, which lead to economic challenges. The issues are yet to be addressed and thus, these particular applications require faster accelerations at the pilot scale, taking into the consideration of the current pandemic and economic issues, for a safer and greener environment. Graphical abstract
This work reports the preparation and characterization of poly(lactic) acid/acrylonitrile butadiene styrene/graphene nanoplatelets/Cloisite C20A montmorillonite (PLA/ABS/GnP/C20A) nanocomposites via melt blending. The clay is hybridized with graphene to increase its dispersion in the polymer matrix. The melt processing temperatures play a vital role in the properties of the resulting nanocomposites in dictating the extent of thermal stability and dispersion of the fillers. The hybrid nanocomposites were characterized for stress-strain, thermal, chemical, and morphological properties. The findings were that there was an increase in the mechanical properties in terms of tensile strength and Young's modulus with the PLA/ABS/GnP/C20A at the high-temperature profile having the highest values of 43.1 MPa and 2533 MPa. The elongation at break increases slightly, due to the brittle properties of GnP. It was found that the dispersion of the fillers increased with increasing temperature profiles, as revealed by the morphological analysis by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The void size was also observed to be smaller and more homogenous with increasing temperature. However, in terms of thermal degradation analysis, the addition of fillers increases its thermal stability as the decomposition onset temperature increases by 22.5 8C.
The objectives of this study were to investigate the most thermodynamically favoured reaction pathway during APR of sorbitol. The thermodynamic analysis of APR of sorbitol was studied using ASPEN Plus V8.0 by applying Gibbs free energy minimization principle, operating at different temperatures (300–800 K), pressure (10–30 bar) and sorbitol concentration (1%, 3%, 5%, 10%, 15% and 20%). The simulation model was validated by comparing the results with the existing work conducted by Serentis and Tsiakaras. The results obtained show that the mol fraction and trend of H2, CO2 and CH4 for both cases are almost similar to the existing work. Therefore the simulation model was validated. Five main reaction pathways of APR of sorbitol were identified and intermediates of each reaction pathway were defined according to their stages and their composition was analyzed. The result obtained show that the decarbonylation reaction (pathway 2) is the most thermodynamically favoured pathway with a total dry basis percentage of 21%.
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