首页> 外文期刊>International journal of hydrogen energy >Analysis of H_2 and CO production via solar thermochemical reacting system of NiFe_2O_4 redox cycles combined with CH_4 partial oxidation
【24h】

Analysis of H_2 and CO production via solar thermochemical reacting system of NiFe_2O_4 redox cycles combined with CH_4 partial oxidation

机译:NiFe_2O_4氧化还原循环结合CH_4部分氧化的太阳热化学反应系统生产H_2和CO的分析

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Thermal reduction of the partial oxidation of CH4-NiFe2O4 followed by oxidation with H2O and CO2 was numerically investigated for H-2 and CO production. P1 radiation model was used to account for radiative heat transfer. The synergistic effect of the reactivity of Fe/Ni exhibited a very promising strategy for producing 45% of syngas with 2.54 ratios of H-2:CO at the first step and 55% of syngas with 2.34 ratios of H-2:CO at the second step. The increase in incident radiation heat flux to 437.69 kW/m(2) resulted in higher reduction kinetics of species conversion until the formation of oxygen carriers consisting of 65% of FeO, 35% of Ni-Fe and 2.6% of carbon deposition. However, during the reduction process, the decrease in total pressure to 0.05 MPa enhanced the species reactivity and the production of H-2 and CO while minimizing carbon deposition. Moreover, the oxidation temperature, operating pressure and the concentration of oxidizing species have strong impacts on the oxidation kinetics. Unlike high thermal reduction process, increasing the total pressure to 1 MPa has favorable effects on syngas production at oxidation step. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:数值研究了热还原CH4-NiFe2O4的部分氧化,然后用H2O和CO2氧化以生产H-2和CO。 P1辐射模型用于说明辐射热传递。 Fe / Ni反应性的协同作用显示出非常有前途的策略,即在第一步生产H2:CO比为2.54的合成气为45%,H-2:CO比为2.34的合成气为55%。第二步。入射辐射热通量增加至437.69 kW / m(2),导致物种转化的还原动力学更高,直到形成由65%的FeO,35%的Ni-Fe和2.6%的碳沉积组成的氧载体。但是,在还原过程中,总压降低到0.05 MPa可以增强物种反应性以及H-2和CO的生成,同时使碳沉积最小。而且,氧化温度,操作压力和氧化物质的浓度对氧化动力学有强烈影响。与高热还原工艺不同,将总压力提高到1 MPa对氧化步骤的合成气生产具有有利的影响。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号