4.7 Article

Sorption enhanced ethanol steam reforming on a bifunctional Ni/CaO catalyst for H2 production

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jece.2021.106725

关键词

Steam reforming; Ethanol; CO2 capture; Hydrogen; Ni/CaO

资金

  1. Spain's Ministry of Science, Innovation and Universities [RTI2018-098283-J-I00, RTI2018-101678-BI00]
  2. Basque Government [IT1218-19, KK-2020/00107]
  3. European Union [823745]
  4. Basque Government
  5. Spain's Ministry of Science and Innovation [PID2019-107357RB-I00]

向作者/读者索取更多资源

The study showed that temperature significantly impacts the performance of the catalyst, with higher temperatures enhancing H2 production in ethanol steam reforming reactions but reducing the catalyst's CO2 capture capacity.
The activity and stability of a 10 wt%NiO/CaO catalyst were tested in the sorption enhanced ethanol steam reforming (SEESR) in a fluidized bed reactor. The effect of temperature in the 600-750 degrees C range was analyzed and the performance of the catalyst at 700 degrees C was assessed by conducting cycles of SEESR reaction and CO2 desorption. At zero time on stream, an increase in temperature enhanced ethanol steam reforming reactions, and therefore H-2 production increased from a yield of 20.3 wt% at 600 degrees C to 22 wt% at 750 degrees C. However, high temperatures hindered the catalyst sorption performance, i.e., CO2 capture declined from 7.9 to 2.1 mmol(CO2) g(cat)(-1). In order to evaluate the catalyst performance throughout the cycles and relate it with its features, both fresh and deactivated catalysts were characterized in detail by N-2 adsorption-desorption, X-ray fluorescence (XRF), X-ray diffraction (XRD), temperature programmed reduction (TPR) and oxidation (TPO) and transmission electron microscopy (TEM). Subsequent to 12 cycles, the catalyst CO2 capture performance was slightly lower than that of the fresh one (approximately 7%) and hardly changed in the next cycles. Furthermore, the use of the same temperature for SEESR reaction and CO2 desorption led to the highest adsorption capacity of the catalyst over multiple cycles.

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