scholarly journals Application of the Alsthom/Exxon alkaline fuel cell system to utility power generation. Final report. [Hydrogen production by catalytic steam reforming of methanol or naphtha]

1977 ◽  
Author(s):  
E. R. Elzinga ◽  
J. G. Bannochie ◽  
R. J. Bellows ◽  
J. H. Correa ◽  
H. H. Horowitz ◽  
...  
Keyword(s):  
Power Generation ◽  
Fuel Cell ◽  
Hydrogen Production ◽  
Steam Reforming ◽  
Cell System ◽  
Final Report ◽  
Alkaline Fuel Cell ◽  
Fuel Cell System ◽  
Steam Reforming Of Methanol ◽  
Catalytic Steam Reforming

A hybrid phosphorus-acid fuel cell system incorporated with oxidative steam reforming of methanol (OSRM) reformer

2020 ◽  
Vol 153 ◽  
pp. 530-538
Author(s):  
Cheng-Ping Chang ◽  
Yen-Chih Wu ◽  
Wei-Yen Chen ◽  
Chin Pan ◽  
Yu-Chuan Su ◽  
...  
Keyword(s):  
Fuel Cell ◽  
Steam Reforming ◽  
Cell System ◽  
Phosphorus Acid ◽  
Fuel Cell System ◽  
Steam Reforming Of Methanol

Synthesis of CuO/ZnO/Al2O3/ZrO2/CeO2 nanocatalysts via homogeneous precipitation and combustion methods used in methanol steam reforming for fuel cell grade hydrogen production

RSC Advances ◽  
2016 ◽  
Vol 6 (62) ◽  
pp. 57199-57209 ◽  
Author(s):  
Saeed Khajeh Talkhoncheh ◽  
Mohammad Haghighi ◽  
Shahab Minaei ◽  
Hossein Ajamein ◽  
Mozaffar Abdollahifar
Keyword(s):  
Fuel Cell ◽  
Hydrogen Production ◽  
Steam Reforming ◽  
Synthesis Method ◽  
Methanol Steam Reforming ◽  
Homogeneous Precipitation ◽  
Steam Reforming Of Methanol

In this research the effects of synthesis method and CeO2 and ZrO2 promoters were studied in the steam reforming of methanol over a CuO/ZnO/Al2O3 nanocatalyst. Addition of ZrO2 and CeO2 reduces CO selectivity, while CeO2 is more effective.

Hydrogen Production for PEM Fuel Cells via Oxidative Steam Reforming of Methanol Using Cu-Al Catalysts Modified With Ce and Cr

2006 ◽  
Author(s):  
Sanjay Patel ◽  
K. K. Pant
Keyword(s):  
Fuel Cell ◽  
Hydrogen Production ◽  
Surface Area ◽  
Steam Reforming ◽  
Pem Fuel Cell ◽  
Oxide Catalysts ◽  
Molar Ratio ◽  
X Ray ◽  
Steam Reforming Of Methanol ◽  
Al Oxide

The performance of Cu-Ce-Al-oxide and Cu-Cr-Al-oxide catalysts of varying compositions prepared by co-precipitation method was evaluated for the PEM fuel cell grade hydrogen production via oxidative steam reforming of methanol (OSRM). The limitations of partial oxidation and steam reforming of methanol for the hydrogen production for PEM fuel cell could be overcome using OSRM and can be performed auto-thermally with idealized reaction stoichiomatry. Catalysts surface area and pore volume were determined using N2 adsorption-desorption method. The final elemental compositions were determined using atomic absorption spectroscopy. Crystalline phases of catalyst samples were determined by X-ray diffraction (XRD) technique. Temperature programmed reduction (TPR) demonstrated that the incorporation of Ce improved the copper reducibility significantly compared to Cr promoter. The OSRM was carried out in a fixed bed catalytic reactor. Reaction temperature, contact-time (W/F) and oxygen to methanol (O/M) molar ratio varied from 200–300°C, 3–21 kgcat s mol−1 and 0–0.5 respectively. The steam to methanol (S/M) molar ratio = 1.4 and pressure = 1 atm were kept constant. Catalyst Cu-Ce-Al:30-10-60 exhibited 100% methanol conversion and 152 mmol s−1 kgcat−1 hydrogen production rate at 300°C with carbon monoxide formation as low as 1300 ppm, which reduces the load on preferential oxidation of CO to CO2 (PROX) significantly before feeding the hydrogen rich stream to the PEM fuel cell as a feed. The higher catalytic performance of Ce containing catalysts was attributed to the improved Cu reducibility, higher surface area, and better copper dispersion. Reaction parameters were optimized in order to maximize the hydrogen production and to keep the CO formation as low as possible. The time-on-stream stability test showed that the Cu-Ce-Al-oxide catalysts subjected to a moderate deactivation compared to Cu-Cr-Al-oxide catalysts. The amount of carbon deposited onto the catalysts was determined using TG/DTA thermogravimetric analyzer. C1s spectra were obtained by surface analysis of post reaction catalysts using X-ray photoelectron spectroscopy (XPS) to investigate the nature of coke deposited.

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