Are Ni/and Ni5Fe1/biochar catalysts suitable for synthetic natural gas production?A comparison with g-Al2O3 supported catalysts

Among challenges implicit in the transition to the post-fossil fuel energetic model,the finite amount of resources available for the technological implementation of CO_(2) revalorizing processes arises as a central issue.The development of fully renewable catalytic systems with easier metal recovery strategies would promote the viability and sustainability of synthetic natural gas production circular routes.Taking Ni and NiFe catalysts supported over g-Al_(2)O_(3) oxide as reference materials,this work evaluates the potentiality of Ni and NiFe supported biochar catalysts for CO_(2) methanation.The development of competitive biochar catalysts was found dependent on the creation of basic sites on the catalyst surface.Displaying lower Turn Over Frequencies than Ni/Al catalyst,the absence of basic sites achieved over Ni/C catalyst was related to the depleted catalyst performances.For NiFe catalysts,analogous Ni_(5)Fe_(1) alloys were constituted over both alumina and biochar supports.The highest specific activity of the catalyst series,exhibited by the NiFe/C catalyst,was related to the development of surface basic sites along with weaker NiFe-C interactions,which resulted in increased Ni0:NiO surface populations under reaction conditions.In summary,the present work establishes biochar supports as a competitive material to consider within the future low-carbon energetic panorama.

Energy Efficiency of a Simulated Synthetic Natural Gas Combined Cycle (SNGCC)

The objective of this investigation is to analyze the impact of the flue gas recirculation (FGR) ratio on the different energy inputs and outputs of a SNGCC power plant as well as its overall efficiency. Simulation results indicate that increasing flue gas recirculation increases the energy consumed by the recirculation compressor and the energy produced by the gas turbine. On the other hand, it decreases the production of energy of the steam turbine and the energy consumed by the pump of the steam cycle. The overall energy efficiency of the SNGCC power plant is highest (41.09%) at a value of 0.20 of the flue gas recirculation. However, the flue gas composition with a FGR ratio of 0.37 is more suitable for effective absorption of carbon dioxide by amine solutions. Based on the low heating value (LHV) of hydrogen, the corresponding overall efficiency of the power plant is 39.18% and the net power output of the plant is 1273 kW for consumption of 97.5 kg/hr. of hydrogen.

Effects of CeO2 preparation methods on the catalytic performance of MoO3/CeO2 toward sulfur-resistant methanation

CeO_2 supports were prepared by calcination or precipitation method and 5% MoO_3/CeO_2 catalysts were prepared by incipient-wetness impregnation method. The catalytic performance of the 5% MoO_3/CeO_2 catalysts toward sulfur-resistant methanation was investigated. The results showed that the Mo/Ce-1 catalysts with CeO_2 support prepared by calcination method exhibited the best sulfur-resistant methanation activity and stability with CO conversion as high as 75% while the Mo/Ce-3 catalysts the poorest. The supports and catalysts were characterized by N_2-adsorption–desorption, temperature-programmed reduction(TPR), X-ray diffraction(XRD), Raman spectroscopy(RS) and scanning electron microscope(SEM). The results indicated that the saturated monolayer loading MoO_3 on Ce-3 support was lower than 5% and there were some crystalline MoO_3 particles on the surface of the Mo/Ce-3. The preparation method of CeO_2 had a big influence on the specific surface area, the crystalline of CeO_2, and the catalytic performance of the corresponding Mo-based catalyst for sulfur-resistant methanation.

Simulation of a NGCC Power Generation Plant for the Production of Electricity from CO2 Emissions Part II: SNGCC Power Plant

The objective of the first part of the investigation was to use Aspen Plus software and the Redlich-Kwong-Soave equation of state in order to simulate an adiabatic methanation reactor for the production of synthetic natural methane (SNG) using 1 kg/hr of carbon dioxide. In this paper, we define the Synthetic Natural Gas Combined Cycle (SNGCC) as a combined cycle power plant where the fuel is synthetic natural gas (SNG) produced by a methanation reactor. The feed of the methanation reactor is the recycled stream of carbon dioxide of a CO2 capture unit treating the flue gas of the SNGCC power plant. The objective of the second part of the investigation is the utilization of Aspen plus software with SRK equation of state for the simulation of the SNGCC power plant. The metallurgical limitation of the gas turbine was fixed at 1300°C in this investigation. For effective absorption by amine solutions, the molar percentage of CO2 in the flue gas should be higher than 10%. Moreover, in order to reduce technical problems linked to oxidative degradation of amine in the CO2 capture plant, the percentage of O2 in the flue gas should also be lower than 5%. To reach this goal, the primary air for combustion has 10% excess air (compared to stoichiometric air) and 37% of the flue gas leaving the SNGCC is recirculated as the secondary air for cooling the turbine. As a result, the concentration of CO2 and O2 of the flue gas entering the CO2 capture unit were respectively equal to 10.2% and 2.01%. The simulation results of the SNGCC power plant indicate that 6.6 MJ of electricity are produced for each kg of carbon dioxide recycled from the CO2 capture unit of the power plant. In other terms, the production of the 24.88 kg/hr of synthetic natural gas (SNG) consumes 62.36 kg/hr of recycled carbon dioxide and 16.4 kg/hr of hydrogen. The SNG produced by the methanation reactor of the power plant generates 114 kW of electricity. It is assumed in this paper that the hydrogen needed for the methanation of carbon dioxide is a product of a catalytic reforming plant that produces gasoline from heavy naphta fraction of an atmospheric distillation unit of crude oil.

La-enhanced Ni nanoparticles highly dispersed on SiC for low-temperature CO methanation performance

For better performances of Ni-based catalysts at low temperatures,Ni/SiC catalyst doped with a little amount of additive La was successfully prepared.The catalytic CO methanation activity tests showed that 3%La-Ni/SiC catalyst was excellent at a low reaction temperature(95.9%CO conversion and 85.1%CH4 selectivity at250℃)with a superior stability compared with Ni/SiC(3.4%CO conversion and 0%CH4 selectivity at 250℃).This can be attributed to that the addition of La can markedly improve the dispersibility of active metal Ni and reduce the particle sizes of Ni nanoparticles or clusters,and can also regulate the interaction between active components and supports.Moreover,the high thermal conductivity and thermal stability could avoid the generation of hot spots in the catalyst bed.These results will promote the development of highly active Ni-based catalysts for the low-temperature methanation reaction.

Characterization and catalytic activity of soft-templated Ni0-CeO_(2) mixed oxides for CO and CO_(2) co-methanation

Nanosized NiO,CeO_(2) and NiO-CeO_(2) mixed oxides with different Ni/Ce molar ratios were prepared by the soft template method.All the samples were characterized by different techniques as to their chemical composition,structure,morphology and texture.On the catalysts submitted to the same reduction pretreatment adopted for the activity tests the surface basic properties and specific metal surface area were also determined.NiO and CeO_(2) nanocrystals of about 4 nm in size were obtained,regardless of the Ni/Ce molar ratio.The Raman and X-ray photoelectron spectroscopy results proved the formation of defective sites at the NiO-CeO_(2) interface,where Ni species are in strong interaction with the support.The microcalorimetric and Fourier transform infrared analyses of the reduced samples highlighted that,unlike metallic nickel,CeO_(2) is able to effectively adsorb CO_(2),forming carbonates and hydrogen carbonates.After reduction in H2 at 400°C for 1 h,the catalytic performance was studied in the CO and CO_(2) co-methanation reaction.Catalytic tests were performed at atmospheric pressure and 300°C,using CO/CO_(2)/H_(2) molar compositions of 1/1/7 or 1/1/5,and space velocities equal to 72000 or 450000 cm^(3)∙h^(-1)∙gcat^(-1).Whereas CO was almost completely hydrogenated in any investigated experimental conditions,CO_(2) conversion was strongly affected by both the CO/CO_(2)/H_(2) ratio and the space velocity.The faster and definitely preferred CO hydrogenation was explained in the light of the different mechanisms of CO and CO_(2) methanation.On a selected sample,the influence of the reaction temperature and of a higher number of space velocity values,as well as the stability,were also studied.Provided that the Ni content is optimized,the NiCe system investigated was very promising,being highly active for the CO_(x) co-methanation reaction in a wide range of operating conditions and stable(up to 50 h)also when submitted to thermal stress.