Single-step synthesized dual-layer hollow fiber membrane reactor for on-site hydrogen production through ammonia decomposition

被引:37
作者
Cheng, Hongda [1 ,2 ]
Meng, Bo [1 ]
Li, Claudia [3 ]
Wang, Xiaobin [1 ]
Meng, Xiuxia [1 ]
Sunarso, Jaka [3 ]
Tan, Xiaoyao [4 ]
Liu, Shaomin [5 ]
机构
[1] Shandong Univ Technol, Sch Chem Engn, Zibo 255049, Peoples R China
[2] Qilu Med Univ, Key Lab Biomed Engn & Technol Univ Shandong, Zibo 255300, Peoples R China
[3] Swinburne Univ Technol, Res Ctr Sustainable Technol, Fac Engn Comp & Sci, Jalan Simpang Tiga, Sarawak 93350, Malaysia
[4] Tianjin Polytech Univ, Dept Chem Engn, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China
[5] Curtin Univ, Dept Chem Engn, Perth, WA 6102, Australia
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Ammonia decomposition; Dual-layer; Hollow fiber; Hydrogen production; Membrane reactor; NI CATALYSTS; GENERATION; PERMEABILITY;
D O I
10.1016/j.ijhydene.2019.04.101
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
On-site hydrogen production via catalytic ammonia decomposition presents an attractive pathway to realize H-2 economy and to mitigate the risk associated with storing large amounts of H-2. This work reports the synthesis and characterization of a dual-layer hollow fiber catalytic membrane reactor for simultaneous NH3 decomposition and H-2 permeation application. Such hollow fiber was synthesized via single-step co-extrusion and co-sintering method and constitutes of 26 mu m-thick mixed protonic-electronic conducting Nd5.5Mo0.5W0.5O11.25-delta (NMW) dense H-2 separation layer and Nd5.5Mo0.5W0.5O11.25-delta Ni (NMW-Ni) porous catalytic support. This dual-layer NMW/NMW-Ni hollow fiber exhibited H2 permeation flux of 0.26 mL cm(-2) min(-1) at 900 degrees C when 50 mL min(-1) of 50 vol% H-2 in He was used as feed gas and 50 mL min(-1) N-2 was used as sweep gas. Membrane reactor based on dual-layer NMW/NMW-Ni hollow fiber achieved NH3 conversion of 99% at 750 degrees C, which was 24% higher relative to the packed-bed reactor with the same reactor volume. Such higher conversion was enabled by concurrent H-2 extraction out of the membrane reactor during the reaction. This membrane reactor also maintained stable NH3 conversion and H-2 permeation flux as well as structure integrity over 75 h of reaction at 750 degrees C. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:7423 / 7432
页数:10
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