Ammonia as an efficient COx-free hydrogen carrier: Fundamentals and feasibility analyses for fuel cell applications

被引:105
作者
Cha, Junyoung [1 ,2 ]
Jo, Young Suk [1 ]
Jeong, Hyangsoo [1 ]
Han, Jonghee [1 ]
Nam, Suk Woo [1 ]
Song, Kwang Ho [2 ,5 ]
Yoon, Chang Won [1 ,3 ,4 ]
机构
[1] KIST, Fuel Cell Res Ctr, 5 Hwarang Ro 14 Gil, Seoul 02792, South Korea
[2] Korea Univ, Green Sch, Anam Ro 145, Seoul 02841, South Korea
[3] Korea Univ Sci & Technol, KIST Sch, Div Energy & Environm Technol, 5 Hwarang Ro 14 Gil, Seoul 02792, South Korea
[4] Kyung Hee Univ, KHU KIST Dept Converging Sci & Technol, 26 Kyungheedae Ro, Seoul 02447, South Korea
[5] Korea Univ, Dept Chem & Biol Engn, 145 Anam Ro, Seoul 02841, South Korea
关键词
Ammonia dehydrogenation; Hydrogen storage; Energy storage; Catalysis Carbon-free energy conversion; Fuel-cell; SODIUM-BOROHYDRIDE; STORAGE MATERIAL; DECOMPOSITION; GENERATION; CATALYSTS; OXIDE; SELECTIVITY; ADSORPTION; CHALLENGES; PROGRESS;
D O I
10.1016/j.apenergy.2018.04.100
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
A COx-free 1 kW-class hydrogen power pack fueled by liquid ammonia is presented. For applications in a practical-scale hydrogen production system in conjunction with a polymer electrolyte membrane fuel cell, Ru catalysts supported on La-doped alumina (Ru/La(x)-Al2O3) were pelletized by varying the lanthanum doping content (x mol%) to control catalytic activities. An optimized Ru(1.06 wt%)/La(20)-Al2O3 pellet catalyst presents a > 99.7% conversion efficiency at 500 degrees C under a gas hourly space velocity of 5000 mL g(cat)(-1)h(-1). Various materials were screened to remove residual ammonia from the product stream, and the X zeolite was chosen as a highly capable adsorbent. Based on the synthesized catalyst and screened adsorbent, a power pack consisting of a dehydrogenation reactor, an adsorbent tower, and a 1 kW-class polymer electrolyte membrane fuel cell was designed and manufactured. The as -integrated system can convert 9 L min(-1) of ammonia into 13.4 L min(-1) of hydrogen, powering a 1 kW-class fuel-cell continuously for > 2 h without any performance degradation. To achieve autothermal and COx-free operations, heat required for ammonia dehydrogenation was provided by unutilized hydrogen from the fuel cell, drastically increasing the overall efficiency of the system to > 49% while removing the external heat source, isobutane. Finally, a drone tethered to the system was operated, demonstrating the feasibility of an elongated flight time of > 4 h, much longer than 14 min with Li-polymer battery loaded on the drone. The system is expected to meet the United States Department of Energy's 2020 gravimetric and volumetric hydrogen storage targets of 4.5 wt% and 30 gH(2) L-1 at system weights of 43 kg and 50 kg, respectively.
引用
收藏
页码:194 / 204
页数:11
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