Hydrogen production from glycerol steam reforming for low- and high-temperature PEMFCs

This paper presents a thermodynamic study of a glycerol steam reforming process, with the aim of determining the optimal hydrogen production conditions for low- and high-temperature proton exchange membrane fuel cells (LT-PEMFCs and HT-PEMFCs). The results show that for LT-PEMFCs, the optimal temperature and steam to glycerol molar ratio of the glycerol reforming process (consisting of a steam reformer and a water gas shift reactor) are 1000 K and 6, respectively; under these conditions, the maximum hydrogen yield was obtained. Increasing the steam to glycerol ratio over its optimal value insignificantly enhanced the performance of the fuel processor. For HT-PEMFCs, to keep the CO content of the reformate gas within a desired range, the steam reformer can be operated at lower temperatures; however, a high steam to glycerol ratio is required. This requirement results in an increase in the energy consumption for steam generation. To determine the optimal conditions of glycerol steam reforming for HT-PEMFC, both the hydrogen yield and energy requirements were taken into consideration. The operational boundary of the glycerol steam reformer was also explored as a basic tool to design the reforming process for HT-PEMFC.     

Thermodynamic analysis of a proton conducting SOFC integrated system fuelled by different renewable fuels

This work proposes a power generation system consisting of steam reformer and SOFC–H⁺ fuelled by different types of fuel, i.e., ethanol, glycerol and biogas. The performance analysis of integrated system is performed based on thermodynamic calculation through Aspen Plus simulator. The total of the Gibbs free energy minimization is used to determine product composition at equilibrium. The electrochemical model not only considers all voltage losses but also includes the effect of current leakage as a result from the electrolyte used. Considering the operating condition of steam reformer, it is found that the gas product contains the highest amount of hydrogen without the carbon formation when reformer is operated at 973 K with steam to carbon ratio of 1. In addition, the simulation results show that the SOFC–H⁺ operated at 973 K and 1 A/cm² can provide a suitable compromise between system performances and exhaust gas composition. The use of glycerol reformate has the highest cell and system efficiencies and fuel utilization compared to the others. In addition, the integrated system fuelled by glycerol can release low CO amount whereas there is more heat provided to the surrounding. Therefore, it can be concluded that glycerol is suitable renewable fuel for SOFC–H⁺ integrated system.     

Performance evaluation of combined solid oxide fuel cells with different electrolytes

The performance of a hybrid system of solid oxide fuel cells with different electrolytes, i.e., an oxygen-ion conducting electrolyte (SOFC-O²⁻) and a proton-conducting electrolyte (SOFC-H⁺) is evaluated in this study. Due to an internal reforming operation, SOFC-O²⁻ can produce electrical power as well as high-temperature exhaust gas containing remaining fuel, i.e., H₂ and CO that can be used for SOFC-H⁺ operation. The remaining CO can further react with H₂O via water gas-shift reaction to produce more H₂ within SOFC-H⁺ and thus, the possibility of carbon formation in SOFC-H⁺ can be eliminated and overall system efficiency can be improved. The simulation results show that the performance of the SOFC-O²⁻–SOFC-H⁺ system provides a higher efficiency (54.11%) compared with the use of a single SOFC. Further, the SOFC hybrid system performance is investigated with respect to important operating conditions, such as temperature, pressure, degree of pre-reforming, inlet fuel velocity, and cell voltage.     

Hydrogen and power generation from supercritical water reforming of glycerol and pressurized SOFC integrated system: Use of different CO2 adsorption process

The performance analysis of an integrated system of glycerol supercritical water reforming and pressurized SOFC was presented. The use of different CO₂ adsorption processes that include in situ and ex situ processes was compared to determine the suitable process for hydrogen and power generations. The influence of operating condition, e.g., temperature and pressure of reformer, supercritical water to glycerol (S/G) molar ratio, and calcium oxide to glycerol (CaO/G) molar ratio was examined. Then, the electrical performance of each integrated process was considered with respect to the SOFC conditions comprising temperature, pressure, and current density. The simulation results revealed that both processes have same favourable conditions for temperature and pressure operated at 800 °C and 240 atm, respectively. The suitable S/G and CaO/G molar ratios for in situ process are 10 and 2 whereas those for ex situ process are 20 and 1. Under these conditions, maximum hydrogen can be achieved as 87% and 75% for in situ and ex situ processes, respectively. When both integrated processes are operated at the optimal SOFC conditions as 900 °C, 4 atm, and current density of 10,000 A/m², the SOFC efficiency of 71.56% and 62.12% can provide for in situ and ex situ processes, respectively.     

Analysis of a pressurized solid oxide fuel cell–gas turbine hybrid power system with cathode gas recirculation

A pressurized solid oxide fuel cell–gas turbine hybrid system (SOFC–GT system) has been received much attention for a distributed power generation due to its high efficiency. When considering an energy management of the system, it is found that a heat input is highly required to preheat air before being fed to the SOFC stack. The recirculation of a high-temperature cathode exhaust gas is probably an interesting option to reduce the requirement of an external heat for the SOFC–GT system. This study aims to analyze the pressurized SOFC–GT hybrid system fed by ethanol with the recycle of a cathode exhaust gas via a simulation study. Effect of important operating parameters on the electrical efficiency and heat management of the system is investigated. The results indicate that an increase in the operating pressure dramatically improves the system electrical efficiency. The suitable pressure is in a range of 4–6 bar, achieving the highest system electrical efficiency and the lowest recuperation energy from the waste heat of the GT exhaust gas. In addition, it is found that the waste heat obtained from the GT is higher than the heat required for the system, leading to a possibility of the SOFC–GT system to be operated at a self-sustainable condition. Under a high pressure operation, the SOFC–GT system requires a high recirculation of the cathode exhaust gas to maintain the system without supplying the external heat; however, the increased recirculation ratio of the cathode exhaust gas reduces the system electrical efficiency.     

Analysis of a proton-conducting SOFC with direct internal reforming

This paper presents a performance analysis of a planar SOFC (solid oxide fuel cell) with proton-conducting electrolyte (SOFC-H⁺). The SOFC-H⁺ is fueled by methane and operated under direct internal reforming and isothermal conditions. A one-dimensional steady-state model coupled with a detailed electrochemical model is employed to investigate the distribution of gas composition within fuel and air channels and all the electrochemical-related variables. The current–voltage characteristics of SOFC-H⁺ are analyzed and the result shows that the operation of SOFC-H⁺ at 0.7 V gives a good compromise on power density and fuel utilization. However, high CO content at fuel channel is observed at this condition and this may hinder the SOFC-H⁺ performance by reducing catalyst activity. The effect of key cell operating parameters, i.e., steam to carbon ratio, temperature, pressure, and water content in oxidant, on the performance of SOFC-H⁺ and the content of CO is also presented in this study.     

用于生产TAEE的反应精馏和全蒸发的混合过程

In this study, a reactive distillation column in which chemical reaction and separation occur simultaneously is applied for the synthesis of tert-amyl ethyl ether （TAEE） from ethanol （EtOH） and tert-amyl alcohol （TAA）. Pervaporation, an efficient membrane separation technique, is integrated with the reactive distillation for enhancing the efficiency of TAEE production. A user-defined Fortran subroutine of a pervaporation unit is developed, allowing the design and simulation of the hybrid process of reactive distillation and pervaporation in Aspen Plus simulator. The performance of such a hybrid process is analyzed and the results indicate that the integration of the reactive distillation with the pervaporation increases the conversion of TAA and the purity of TAEE product, compared with the conventional reactive distillation.     

Using a membrane reactor for the oxidative coupling of methane: simulation and optimization

An oxidative coupling of methane (OCM) is a promising process to convert methane into ethylene and ethane; however, it suffers from the relatively low selectivity and yield of ethylene at high methane conversion. In this study, a membrane reactor is applied to the OCM process in order to prevent the deep oxidation of a desirable ethylene product. The mathematical model of OCM process based on mass and energy balances coupled with detailed OCM kinetic model is employed to examine the performance of OCM membrane reactor in terms of CH₄ conversion, C₂ selectivity, and C₂ yield. The influences of key operating parameters (i.e., temperature, methane-to-oxygen feed ratio, and methane flow rate) on the OCM reactor performance are further analyzed. The simulation results indicate that the OCM membrane reactor operated at higher operating temperature and lower methane-to-oxygen feed ratio can improve C₂ production. An optimization of the OCM membrane reactor using a surface response methodology is proposed in this work to determine its optimal operating conditions. The central composite design is used to study the interaction of process variables (i.e., temperature, methane-to-oxygen feed ratio, and methane flow rate) and to find the optimum process operation to maximize the C₂ products yield.     

Adsorption-membrane hybrid system for ethanol steam reforming: Thermodynamic analysis

In this study, an adsorption-membrane hybrid system in which a carbon dioxide adsorbent is used to remove undesired carbon dioxide and a membrane is applied for hydrogen separation is theoretically investigated with the aim to improve the performance of an ethanol steam reforming. A thermodynamic analysis of such the system was performed and compared with a membrane reactor and an adsorptive reactor. It was found that the removal of hydrogen by membrane separation has higher impact on the reformer performance than the carbon dioxide capture by adsorption. The adsorption-membrane hybrid system for ethanol steam reforming gives the highest hydrogen yield. Considering a possibility for carbon formation, the simulation results showed that the use of membrane for pure hydrogen production increases the trend toward carbon formation. This is due to an increase in carbon monoxide concentration in the reaction zone that promotes the Boudouard reaction. In contrast, the use of carbon dioxide adsorbent reduces the formation of carbon as carbon monoxide is less generated in the system.