Reaction Characteristics of Ce-Based Oxygen Carrier for Two-Step Production Syngas and Hydrogen through Methane Conversion and Water Splitting

2013 ◽  
Vol 641-642 ◽  
pp. 123-127
Author(s):  
Yong Gang Wei ◽  
Xing Zhu ◽  
Kong Zhai Li ◽  
Ya Ne Zheng ◽  
Hua Wang

The two-step steam methane reforming for production syngas and hydrogen was investigated by using Ce-based oxygen carriers (CeO2, CeO2-ZrO2,CeO2-Fe2O3) which were prepared by co-precipitation method and characterized by means of X-ray diffractometer and Raman spectroscopy. CH4 temperature programmed and isothermal reactions were adopted to test syngas production reactivity, and redox properties were evaluated by a successive redox cycle. The results showed that the incorporation of ZrO2 into CeO2 was found to be an effective approach for enhancing the reducibility of CeO2 in methane conversion reaction and redox performance, and the addition of Fe2O3 into CeO2 could obviously increase the amount of reactive oxygen species in CeO2-Fe2O3 and the yields of syngas and hydrogen reached maximum in the 3rd cycle, but the redox stability of CeO2-Fe2O3 needs to be enhanced.

2021 ◽  
Vol 11 (10) ◽  
pp. 4713
Author(s):  
Carlos Arnaiz del Pozo ◽  
Schalk Cloete ◽  
Ángel Jiménez Álvaro ◽  
Felix Donat ◽  
Shahriar Amini

The hydrogen economy has received resurging interest in recent years, as more countries commit to net-zero CO2 emissions around the mid-century. “Blue” hydrogen from natural gas with CO2 capture and storage (CCS) is one promising sustainable hydrogen supply option. Although conventional CO2 capture imposes a large energy penalty, advanced process concepts using the chemical looping principle can produce blue hydrogen at efficiencies even exceeding the conventional steam methane reforming (SMR) process without CCS. One such configuration is gas switching reforming (GSR), which uses a Ni-based oxygen carrier material to catalyze the SMR reaction and efficiently supply the required process heat by combusting an off-gas fuel with integrated CO2 capture. The present study investigates the potential of advanced La-Fe-based oxygen carrier materials to further increase this advantage using a gas switching partial oxidation (GSPOX) process. These materials can overcome the equilibrium limitations facing conventional catalytic SMR and achieve direct hydrogen production using a water-splitting reaction. Results showed that the GSPOX process can achieve mild efficiency improvements relative to GSR in the range of 0.6–4.1%-points, with the upper bound only achievable by large power and H2 co-production plants employing a highly efficient power cycle. These performance gains and the avoidance of toxicity challenges posed by Ni-based oxygen carriers create a solid case for the further development of these advanced materials. If successful, results from this work indicate that GSPOX blue hydrogen plants can outperform an SMR benchmark with conventional CO2 capture by more than 10%-points, both in terms of efficiency and CO2 avoidance.


2017 ◽  
Vol 42 (1) ◽  
pp. 8-13 ◽  
Author(s):  
Yubo Ma ◽  
Zhixian Gao ◽  
Wumanjiang Eli

Rh catalysts supported on Fe2O3, Co3O4 and Fe2O3–Co3O4 mixed oxide were prepared by the co-precipitation method. The effect of the support on the performance of the Rh catalysts for the hydroformylation of dicyclopentadiene was investigated using X-ray photoelectron spectroscopy, H2-temperature-programmed reduction, H2-temperature-programmed desorption and Brunauer–Emmett–Teller analysis techniques. The results indicated that the Fe2O3–Co3O4 supported catalyst had a higher dispersion of Rh and thus more Rh+ sites. As a result, the Fe2O3–Co3O4 supported Rh catalyst exhibited higher activity compared with counterparts supported on Fe2O3 and Co3O4.


2017 ◽  
Vol 23 (1) ◽  
pp. 49-56 ◽  
Author(s):  
Yajing Zhang ◽  
Yu Zhang ◽  
Fu Ding ◽  
Kangjun Wang ◽  
Wang Xiaolei ◽  
...  

A series of La2O3-modified CuO-ZnO-ZrO2/HZSM-5 catalysts were prepared by an oxalate co-precipitation method. The catalysts were fully characterized by X-ray diffraction (XRD), N2 adsorption-desorption, hydrogen temperature pro-grammed reduction (H2-TPR), ammonia temperature programmed desorption (NH3-TPD), and X-ray photoelectron spectroscopy (XPS) techniques. The effect of the La2O3 content on the structure and performance of the catalysts was thoroughly investigated. The catalysts were evaluated for the direct synthesis of dimethyl ether (DME) from CO2 hydrogenation. The results displayed that La2O3 addition enhanced catalytic performance, and the maximal CO2 conversion (34.3%) and DME selectivity (57.3%) were obtained over the catalyst with 1% La2O3, which due to the smaller size of Cu species and a larger ratio of Cu+/Cu.


2021 ◽  
Vol 12 (1) ◽  
pp. 391
Author(s):  
Haiming Gu ◽  
Juan Yang ◽  
Guohui Song ◽  
Xiaobo Cui ◽  
Miaomiao Niu ◽  
...  

Chemical looping biomass gasification is a novel technology converting biomass into syngas, and the selection of oxygen carrier is key for efficient tar conversion. The performance of LaFe1-xNix as a robust catalytic oxygen carrier was investigated in the chemical looping conversion of toluene (tar model compound) into syngas in a fixed bed. LaM (M = Fe, Ni, Mn, Co, and Cu) was initially compared to evaluate the effect of transition metal on toluene conversion. LaFe (partial oxidation) and LaNi (catalytic pyrolysis) exhibited better performance in promoting syngas production than other oxygen carriers. Therefore, Ni-substituted ferrite LaFe1-xNix (x = 0, 0.2, 0.4, 0.6, 0.8 and 1) was further developed. The effects of Ni-substitution, steam/carbon ratio (S/C), and temperature on toluene conversion into C1 and H2 were evaluated. Results showed that the synergistic effect of Fe and Ni promoted toluene conversion, improving H2 yield yet with serious carbon deposition. Steam addition promoted toluene steam reforming and carbon gasification. With S/C increasing from 0.8 to 2.0, the C1 and H2 yield increased from 73.9% to 97.5% and from 197.7% to 269.6%, respectively. The elevated temperature favored toluene conversion and C1 yield. LaFe0.6Ni0.4 exhibited strong reactivity stability during toluene conversion at S/C = 1.6 and 900 °C.


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