Statistical Method of Deducting Activation Energies for the Steam Methane Reforming Reactions

In this paper, a method of deducting activation energies for heterogeneous reactions of steam methane reforming is presented. The essence of the method lies in iterative evaluation of kinetic parameters, namely activation energies of reactions, for a given reactor. The novelty of the method lies in utilizing a statistical approach to reduce computational effort of numerical simulation. The method produces multivariable correlations between activation energies and operational parameters of the process: pressure, temperature, steam-to-methane ratio, residence time, and catalyst properties. These correlations can be used for numerical simulations of steam methane reforming to yield methane conversion rate, spatial and temporal distribution of reaction products, temperature and pressure within the reactor. An average computational effort is equal to a batch of 18 ([Formula: see text]) simulations for [Formula: see text] variables. The method was demonstrated by evaluating two-variable correlations of activation energies with pressure and temperature. The developed numerical model was validated against adopted experimental data.

The Role of Strontium in CeNiO3 Nano-Crystalline Perovskites for Greenhouse Gas Mitigation to Produce Syngas

The transition metal-based catalysts for the elimination of greenhouse gases via methane reforming using carbon dioxide are directly or indirectly associated with their distinguishing characteristics such as well-dispersed metal nanoparticles, a higher number of reducible species, suitable metal–support interaction, and high specific surface area. This work presents the insight into catalytic performance as well as catalyst stability of CexSr1−xNiO3 (x = 0.6–1) nanocrystalline perovskites for the production of hydrogen via methane reforming using carbon dioxide. Strontium incorporation enhances specific surface area, the number of reducible species, and nickel dispersion. The catalytic performance results show that CeNiO3 demonstrated higher initial CH4 (54.3%) and CO2 (64.8%) conversions, which dropped down to 13.1 and 19.2% (CH4 conversions) and 26.3 and 32.5% (CO2 conversions) for Ce0.8Sr0.2NiO3 and Ce0.6Sr0.4NiO3, respectively. This drop in catalytic conversions post strontium addition is concomitant with strontium carbonate covering nickel active sites. Moreover, from the durability results, it is obvious that CeNiO3 exhibited deactivation, whereas no deactivation was observed for Ce0.8Sr0.2NiO3 and Ce0.6Sr0.4NiO3. Carbon deposition during the reaction is mainly responsible for catalyst deactivation, and this is further established by characterizing spent catalysts.

Effect of Ruthenium and Cerium Oxide (IV) Promotors on the Removal of Carbon Deposit Formed during the Mixed Methane Reforming Process

This work investigates the effect of the addition of Ru and CeO2 on the process of gasification of carbon deposits formed on the surface of a nickel catalyst during the mixed methane reforming process. Activity studies of the mixed methane reforming process were carried out on (Ru)-Ni/CeO2-Al2O3 catalysts at the temperature of 650–750 °C. The ruthenium-promoted catalyst exhibited the highest activity. Carbonized post-reaction catalyst samples were tested with the TOC technique to investigate the carbonization state of the samples. The bimetallic catalyst had the lowest amount of carbon deposit (1.5%) after reaction at 750 °C. The reactivity of the carbon species was assessed in mixtures of oxygen, hydrogen, carbon dioxide, and water. Regardless of the gasifying agent used, the carbon deposit was removed from the surface of the catalytic system. The overall mechanism of mixed methane reforming over Ru and CeO2 was shown.

Techno-Economic Evaluation of Hydrogen Production via Gasification of Vacuum Residue Integrated with Dry Methane Reforming

The continuous rise of global carbon emissions demands the utilization of fossil fuels in a sustainable way. Owing to various forms of emissions, our environment conditions might be affected, necessitating more focus of scientists and researchers to upgrade oil processing to more efficient manner. Gasification is a potential technology that can convert fossil fuels to produce clean and environmentally friendly hydrogen fuel in an economical manner. Therefore, this study analyzed and examined it critically. In this study, two different routes for the produc-tion of high-purity hydrogen from vacuum residue while minimizing the carbon emissions were proposed. The first route (Case I) studied the gasification of heavy vacuum residue (VR) in series with dry methane reforming (DMR). The second route studied the gasification of VR in parallel integration with DMR (Case II). After investigating both processes, a brief comparison was made between the two routes of hydrogen production in terms of their CO2 emissions, en-ergy efficiency, energy consumption, and environmental and economic impacts. In this study, the two vacuum-residue-to-hydrogen (VRTH) processes were simulated using Aspen Plus for a hydrogen production capacity of 50 t/h with 99.9 wt.% purity. The results showed that Case II offered a process energy efficiency of 57.8%, which was slightly higher than that of Case I. The unit cost of the hydrogen product for Case II was USD 15.95 per metric ton of hydrogen, which was almost 9% lower than that of Case I. In terms of the environmental analysis, both cases had comparably low carbon emissions of around 8.3 kg of CO2/kg of hydrogen produced; with such high purity, the hydrogen could be used for production of other products further downstream or for industrial applications.