Development of highly efficient methanol steam reforming system for hydrogen production and supply for a low temperature proton exchange membrane fuel cell

Methanol steam reforming (MSR) has been regarded as a promising hydrogen supply method for proton exchange membrane fuel cell (PEMFC), while the efficiency for hydrogen production and integration method of MSR with PEMFC are two major challenges for commercial applications. Here, we present a highly efficient MSR system for hydrogen production and supply for low temperature PEMFC (LT-PEMFC). The MSR system has a highly compact microreactor, wherein MSR, methanol combustion, and CO selective methanation reactions occur. The CO selective methanation is used to reduce the content of CO concentration to remit the CO poison, then the reformate of MSR system is mixed with air and supply for the LT-PEMFC. Then, experimental tests are conducted to investigate the effects of operating parameters on hydrogen production. A staged supply strategy is proposed, it enables to startup the system within 11.2 min and with methanol consumption of 34.72 g. Results show that the methanol conversion can reach up to 93.0% and system's energy efficiency of 76.2%. After integration with a LT-PEMFC, a maximum 160 W electricity can be generated. The results obtained in this study demonstrated that the developed MSR system can be used to supply hydrogen for LT-PEMFC and able to power mobile device requiring hundreds of watts power consumption.     

Development of methanol steam reforming microreactor based on stacked wave sheets and copper foam for hydrogen production

Methanol steam reforming has been used for in-situ hydrogen production and supply for proton exchange membrane fuel cell (PEMFC), while its power density and energy efficiency still needs to be improved. Herein, we present a novel methanol steam reforming microreactor based on the stacked wave sheets and copper foam for highly efficient hydrogen production. The structural of stacked wave sheets and copper foam, and their roles in the microreactor are described, methanol catalytic combustion is adopted to supply heat for methanol steam reforming reaction and enables the microreactor to work automatically. For catalyst carrier, a fractal body-centered cubic model is established to study the flow characteristics and chemical reaction performances of the copper foam with coated catalyst layer. Both simulation and experimental results showed that the reformate flowrate increases with the increasing of microreactor layers and methanol solution flowrate, the discrepancies of methanol conversion between simulation and experimental tests are less than 7%. Experimental results demonstrated that the reformate flowrate of 1.0 SLM can be achieved with methanol conversion rate of 65%, the output power of the microreactor is 159 W and power density is 395 W/L. The results obtained in this study indicates that stacked wave sheets and copper foam can uniform the reactant flow and improve the hydrogen production performances.     

Experiments on hydrogen production from methanol steam reforming in the microchannel reactor

The entire experiments were conducted for microchannel methanol steam reforming, by which, the selection of catalyst, the operating parameters and the configuration of microchannels were discussed thoroughly. It was found that the higher the Cu concentration is, the more the corresponding active surface area of Cu will be, thereby improving the catalytic activity. The Cu-to-Zn ratio in Cu/ZnO/Al₂O₃ catalyst should be set at 1:1. The impacts of reaction temperature, feed flow rate, mixture temperature, and H₂O-to-CH₃OH molar ratio on the methanol conversion rate were also revealed and discussed. Characteristics of micro-reactors with various microchannels, including that 20 mm and 50 mm in length, as well as non-parallel microchannels, were investigated. It was found that the increase of microchannel length can improve the methanol conversion rate significantly. Besides, non-parallel microchannels help to maintain flow and temperature distribution uniformity, which can improve the performance of micro-reactor. In the present experiments, the presence of CO was under the condition that the methanol conversion rate was above 70%.     

Underwater vehicle hydrogen production from methanol steam reforming using hydrogen peroxide

Methanol steam reforming (MSR) can supply hydrogen (H₂) to underwater vehicles equipped with a fuel cell. Low reaction temperatures ensure the composition of the reformed gas suitable for the H₂ purification unit and increase the design freedom of a reforming plant. However, such temperatures decrease the catalyst activity and thereby the methanol (MeOH) conversion and H₂ production. Herein, hydrogen peroxide (H₂O₂) was supplied with MeOH and water (H₂O) to ensure sufficient MeOH conversion and H₂ production at low temperatures. A tube reactor loaded with a commercial Cu/Zn catalyst was installed in an electric furnace maintained at 200–250 °C, and MeOH and 0 wt%, 11.88 wt%, 22.51 wt%, and 32.07 wt% H₂O₂ were supplied. When the furnace temperature was 200 °C, the MeOH conversion was 49.3% at 0 wt% H₂O₂ but 93.5% at 32.07 wt% H₂O₂. The effect of adding H₂O₂ was greater under the temperature conditions where the MeOH conversion was 100% or less. To analyze the effect of H₂O₂ addition on catalyst durability, the furnace was maintained at 200 °C, and the reactor was continuously operated for 110 h with 0 wt% and 32.07 wt% H₂O₂. The addition of H₂O₂ did not significantly decrease the Cu/Zn catalyst durability.     

Microwave-activated methanol steam reforming for hydrogen production

Methanol steam reforming (MSR) was carried out in a catalytic packed bed reactor under electrical and microwave heating using the two most common catalysts for this process-CuZnO/Al₂O₃ and PdZnO/Al₂O₃. Significant two-dimensional temperature gradients were found, especially in the latter case. Our results show that for the same average bed temperature, methanol conversion is higher under microwave heating (>10%). On the other hand, the product distribution is not affected by the heating mode. We demonstrate that even in cases where the maximum temperature along the entire height of the bed is significantly higher under electrical heating, conversion is either higher in the microwave case or approximately the same between the two heating modes. Finally, our experimental data indicate that a given methanol conversion can be achieved with lower net heat input to the reactor under microwave heating. This does not mean lower total energy consumption in the microwave process due to the limitations in the magnetron efficiency and the reflected power. However, it may be an implicit indication of higher temperature at metal sites than in bulk phase (microscale hot spot formation) due to the selective heating principle.     

Porous copper fiber sintered felts with surface microchannels for methanol steam reforming microreactor for hydrogen production

In this study, a laser micro-milling technique was introduced into the fabrication process of surface microchannels with different geometries and dimensions on the porous copper fiber sintered felts (PCFSFs). The PCFSFs with surface microchannels as catalyst supports were then used to construct a new type of laminated methanol steam reforming microreactor for hydrogen production. The microstructure morphology, pressure drop, velocity and permeability of PCFSF with surface microchannels were studied. The effect of surface microchannel shape (rectangular, stepped, and polyline) and catalyst loading amount on the reaction performance of methanol steam reforming microreactor for hydrogen production was further investigated. Our results show that the PCFSF with rectangular microchannels demonstrated a lower pressure drop, higher average velocity and higher permeability compared to the stepped and polyline microchannel. Furthermore, the PCFSF with rectangular microchannels also exhibited the highest methanol conversion and H₂ flow rate. The best reaction performance of methanol steam reforming microreactor for hydrogen production was obtained using PCFSF with rectangular microchannels when 0.5 g catalyst was loaded.     

Performance assessment and evaluation of catalytic membrane reactor for pure hydrogen production via steam reforming of methanol

The steam reforming of methanol was investigated in a catalytic Pd–Ag membrane reactor at different operating conditions on a commercial Cu/ZnO/Al₂O₃ catalyst. A comprehensive two-dimensional non-isothermal stationary mathematical model has been developed. The present model takes into account the main chemical reactions, heat and mass transfer phenomena in the membrane reactor with hydrogen permeation across the PdAg membrane in radial direction. Model validation revealed that the predicted results satisfy the experimental data reasonably well under the different operating conditions. Also the impact of different operating parameters including temperature, pressure, sweep ratio and steam ratio on the performance of reactor has been examined in terms of methanol conversion and hydrogen recovery. The modeling results have indicated the high performance of the membrane reactor which is related to continuous removal of hydrogen from retentate side through the membrane to shift the reaction equilibrium towards formation of hydrogen. The obtained results have confirmed that increasing the temperature improves the kinetic properties of the catalyst and increase in the membrane's H₂ permeance, which results in higher methanol conversion and hydrogen production. Also it is inferred that the hydrogen recovery is favored at higher temperature, pressure, sweep ratio and steam ratio. The model prediction revealed that at 573 K, 2 bar and sweep ratio of 1, the maximum hydrogen recovery improves from 64% to 100% with increasing the steam ratio from 1 to 4.     

A review on reforming bio-ethanol for hydrogen production

Bio-ethanol is a prosperous renewable energy carrier mainly produced from biomass fermentation. Reforming of bio-ethanol provides a promising method for hydrogen production from renewable resources. Besides operating conditions, the use of catalysts plays a crucial role in hydrogen production through ethanol reforming. Rh and Ni are so far the best and the most commonly used catalysts for ethanol steam reforming towards hydrogen production. The selection of proper support for catalyst and the methods of catalyst preparation significantly affect the activity of catalysts. In terms of hydrogen production and long-term stability, MgO, ZnO, _CeO2${\mathrm{CeO}}_2$, and _La2O3${\mathrm{La}}_2{\mathrm{O}}_3$ are suitable supports for Rh and Ni due to their basic characteristics, which favor ethanol dehydrogenation but inhibit dehydration. As Rh and Ni are inactive for water gas shift reaction (WGSR), the development of bimetallic catalysts, alloy catalysts, and double-bed reactors is promising to enhance hydrogen production and long-term catalyst stability. Autothermal reforming of bio-ethanol has the advantages of lesser external heat input and long-term stability. Its overall efficiency needs to be further enhanced, as part of the ethanol feedstock is used to provide low-grade thermal energy. Development of millisecond-contact time reactor provides a low-cost and effective way to reform bio-ethanol and hydrocarbons for fuel upgrading. Despite its early R&D stage, bio-ethanol reforming for hydrogen production shows promises for its future fuel cell applications.     

A novel thermally autonomous methanol steam reforming microreactor using SiC honeycomb ceramic as catalyst support for hydrogen production

Methanol steam reforming (MSR) is an attractive option for in-situ hydrogen production and to supply for transportation and industrial applications. This paper presents a novel thermally autonomous MSR microreactor that uses silicon carbide (SiC) honeycomb ceramic as a catalyst support to enhance energy conversion efficiency and hydrogen production. The structural design and working principle of the MSR microreactor are described along with the development of a 3D numerical model to study the heat transfer and fluid flow characteristics. The simulation results indicate that the proposed microreactor has a significantly low drop in pressure and more uniform temperature distribution in the SiC ceramic support. Further, the microreactor was developed and an experimental setup was conducted to test its hydrogen production performance. The experimental results show that the developed microreactor can be operated as thermally autonomous to reach its target working temperature within 9 min. The maximum energy efficiency of the microreactor is 67.85% and a hydrogen production of 316.37 ml/min can be achieved at an inlet methanol flow rate of 360 μl/min. The obtained results demonstrate that SiC honeycomb ceramic with high thermal conductivity can serve as an effective catalyst support for the development of MSR microreactors for high volume and efficient hydrogen production.     

Oxidative pyrolysis reforming of methanol in warm plasma for an on-board hydrogen production

To achieve on-board hydrogen production with high energy efficiency and low energy cost, the oxidative pyrolysis reforming (OPR) of methanol using air as an oxidant in a heat-insulated gliding arc plasma reactor is explored. Effects of dioxygen/methanol (O₂/C) ratio, steam/methanol (S/C) ratio and specific energy input (SEI) on the OPR are investigated. The reaction rate ratio (α) of pyrolysis reforming to oxidative reforming in the OPR is deduced. The OPR of methanol strongly depends on the O₂/C ratio, with which methanol conversion increases rapidly. In the OPR, methanol conversions occur mainly by the oxidative reforming (partial oxidation) at the O₂/C ratios below 0.20, but by the oxidative reforming and the promoted pyrolysis reforming at the O₂/C ratios above 0.20, which is confirmed by the enthalpy change for the overall reaction of OPR. Higher O₂/C ratio results in higher energy efficiency and lower energy cost, however, higher S/C ratio or larger SEI leads to lower energy efficiency and higher energy cost. Under conditions of O₂/C = 0.30, S/C = 0.5, SEI = 24 kJ/mol, energy efficiency of 74% and energy cost of 0.45 kWh/Nm³ with methanol conversion of 88% are achieved.     

Co-current and counter-current modes for methanol steam reforming membrane reactor

In this simulation study, methanol steam reforming reaction to produce synthesis gas has been studied in a membrane reactor when shell side and lumen side streams are in co-current mode or in counter-current mode. The simulation results for both co-current and counter-current modes are presented in terms of methanol conversion and molar fraction versus temperature, pressure, _H2O/_CH3OH${\mathrm{H}}_2\mathrm{O}/{\mathrm{CH}}_3\mathrm{OH}$ molar feed flow rate ratio and axial co-ordinate.     

Modeling and simulation of microwave double absorption on methanol steam reforming for hydrogen production

Methanol steam reforming (MSR) accompanied by methanol decomposition (MD) in an environment with microwave heating is modeled and simulated numerically in the present study. In the developed method, the governing equations simultaneously consider the continuity, momentum, energy, species and Maxwell’s equations. Meanwhile, the double absorption of microwaves by both the reactants and the catalyst bed in the reactor is also taken into account. The heating processes of microwaves on the reactants and the catalyst bed are described by establishing two sets of complex relative permittivity in the non-porous and porous region. The permittivity consists of a dielectric constant and a dielectric loss factor. The obtained results indicate that the developed model can predict MSR and MD accurately. With microwave irradiation, it is found that varying dielectric loss factor in the non-porous region has a significant impact on hydrogen production, revealing that the preheating of the reactants plays a prominent role in determining the performance of MSR. Regarding microwave power, it is observed that increasing power intensifies H₂ yield, especially at 500 W where methanol is depleted completely. However, an increase in power also makes MD tend to grow in that the CO₂ selectivity decreases.     

Integrated methanol reforming and oxidation in wash-coated microreactors: A three-dimensional simulation

A microreactor consisting of two parallel channels is numerically simulated where methanol steam reforming takes place in one channel, and the required heat is supplied by methanol oxidation in the other channel. Effects of different parameters on methanol conversion, hydrogen yield and CO concentration are examined. Results from the parametric study are then used to propose conditions for high methanol conversion and hydrogen yield. A microreactor with enhanced output conditions is thus designed which is capable of producing a gas stream consisting of 74% hydrogen (dry). CO concentration in the generated synthesis gas stream is low enough to require only a PROX reactor for CO clean-up, eliminating the need for a bulky water–gas shift reactor. The produced hydrogen from an assembly of such microreactors can feed a low-power PEM fuel cell. A cluster of these microreactors would take a volume of about 91 cm³ to feed a typical 30-watt PEM fuel cell.     

On-board methanol catalytic reforming for hydrogen Production-A review

Hydrogen has become a versatile and clean alternative to meet increasingly urgent energy demands since its high heating value and renewability. However, considering the hazards of hydrogen storage and transport, in-situ production processes are drawing more attention. Among all the hydrogen carriers, methanol has become one of the research focuses due to its high H/C ratio, flexibility and sustainability. Regarded as the core of hydrogen supply system, catalysts with higher activity, selectivity and stability are continuously developed for improved efficiency. In this review, two groups of catalysts were investigated namely copper-based and group VIII metal-based catalysts. Not only macro indicators such as feedstock conversion and product selectivity, but also micro interaction and reaction mechanism were elaborated, with respect to the effects of promoters, supports, synthesis methods and binary metal components. Notably, several reaction pathways and catalysts deactivation mechanisms were suggested based on this series of inspection of the structure-reactivity relationship, along with a general perception that large surface area, well dispersed metals, small particle size and synergy effects significantly improve the catalytic performance. Accordingly, a novel concept of single-atom catalysts (SACs) was introduced aimed at efficient hydrogen production under more moderate conditions, by combining the advantages of heterogeneous and homogeneous catalysis. Additionally, an efficient reforming process is required by properly regulating the feed flow and heat flow through a coupled system. Conclusively, a thorough supply and demand network of hydrogen based on methanol was presented, giving an overview for on-board applications of hydrogen energy.     

Experiments on hydrogen production from methanol steam reforming in fluidized bed reactor

A novel approach for the hydrogen production which integrated methanol steam reforming and fluidized bed reactor (FBR) was proposed. The reaction was carried out over Cu/ZnO/Al₂O₃ catalysts. The critical fluidized velocities under different catalyst particle sizes and masses were obtained. The influences of the operating parameters, including that of H₂O-to-CH₃OH molar ratio, feed flow rate, reaction temperature, and catalyst mass on the performance of methanol steam reforming were investigated in FBR to obtain the optimum experimental conditions. More uniform temperature distribution, larger surface volume ratio and longer contacting time can be achieved in FBR than that in fixed bed reactor. The results indicate that the methanol conversion rate in FBR can be as high as 91.95% while the reaction temperatures is 330 °C, steam-to-carbon molar ratio is 1.3, and feed flow rate is 540 ml/h under the present experiments, which is much higher than that in the fixed bed.     

Morphology effect of ceria on the performance of CuO/CeO2 catalysts for hydrogen production by methanol steam reforming

Nano-rod(R), nano-particle(P) and sponginess(S) of ceria samples were used to study catalytic performance of hydrogen production by methanol steam reforming. The samples were prepared by hydrothermal method, precipitation method, and sol-gel method, respectively, and the CuO was supported on the different morpholopy of CeO₂ samples by wet impregnation. SEM, TEM, XRD, XRF, BET, H₂-TPR, XPS and N₂O titration methods were used to study correlation between the structure and the catalytic performance for methanol steam reforming. The results showed that the morphology of the prepared CeO₂ support dramatically influenced the performance of catalysts. Due to the stronger interaction between copper oxide and ceria support, the CuO/CeO₂-R catalyst had exhibited the better catalytic activity than those of the CuO/CeO₂P and CuO/CeO₂S catalysts. Moreover, higher Cu dispersion, lower reduction temperature of CuO, and higher content of active species Cu⁺ were also advantageous to raising catalytic effects. Besides, with the highest content of surface Ce³⁺, the CuO/CeO₂-R had estimated the content of oxygen vacancy on the surface of the catalyst. The existence of surface oxygen vacancy had a positive effect on the methanol steam reforming.     

Numerical predictions of design and operating parameters of reformer on the fuel conversion and CO production for the steam reforming of methanol

SIMPLE-C algorithm and Arrhenius form of reaction model were employed to simulate the three-dimensional laminar flow field and the chemical reaction in a cylindrical methanol reformer under steam reforming. The effects of geometrical and thermo-fluid parameters on the CO and CO₂ productions as well as the heat and mass transfer in a cylindrical methanol reformer with a constant-volume catalyst bed will be observed in the present study. Low CO concentration in hydrogen-rich gas denotes a low load of CO removal in purifying processes. The results indicate that the smaller diameter-to-length ratio of chamber with a thicker catalyst bed enhances the methanol conversion and reduces the overall CO concentration in the cylindrical methanol reformer. This is because that a lower temperature distribution restrains the reverse water–gas-shift reaction to reduce the production of CO with a thicker catalyst bed.     

The progress in water gas shift and steam reforming hydrogen production technologies – A review

Hydrogen has been widely considered a clean fuel of the future, with the highest mass based energy density of known fuels. Water gas shift (WGS) and steam reforming (SR) are the major reactions used for hydrogen production, and improved catalysts are essential to the future of the WGS and SR processes. Much progress in the different aspects of these fields has been made recently, which includes approaches to preparation and characterization, doping and promotion, as well as evaluation of catalysts, especially nanocatalysts. Significant improvements have been realized in increasing the stability of the catalysts, the overall conversion of raw materials, and the hydrogen production selectivity. This review aims to introduce these hydrogen production processes, to present developments in these areas, and discusses recent improvements that have made noteworthy impacts.     

Robust multi-objective optimization of methanol steam reforming for boosting hydrogen production

Methanol steam reforming (MSR) has been considered as a promising method for producing pure hydrogen in recent decades. A comprehensive two-dimensional steady-state mathematical model was developed to analyze the MSR reactor. To improving high purity hydrogen production, a triple-objective optimization of the MSR reactor is performed. Non-dominated Sorting Genetic Algorithm-II (NSGA-II) is employed as a robust optimization approach to maximize the three objectives, termed as, methanol conversion, CO selectivity, and H₂ selectivity. The Pareto optimal frontier has also been provided and the ultimate solution of the Pareto front has been found by the three decision-making methods (TOPSIS, LINMAP, and Shannon's Entropy). Among the three distinct decision-making approaches, LINMAP presents better results according to the deviation index parameter. It has been shown that a perfect agreement is available between the plant and simulation data. Operating under the optimum values based on the LINMAP method confirms an almost 47.04% enhancement of H₂ mass fraction compared to the conventional industrial MSR reactor. The predicted results advocate that the key superiority of the optimized-industrial reactor is the remarkable higher production rate of hydrogen compared to the conventional MSR reactor which makes optimized-industrial reactor both feasible and beneficial.