TY - JOUR
T1 - Enhanced ammonia-cracking process via induction heating for green hydrogen
T2 - A comprehensive energy, exergy, economic, and environmental (4E) analysis
AU - Yun, Seunggwan
AU - Im, Junhyeok
AU - Kim, Junhwan
AU - Cho, Hyungtae
AU - Lee, Jaewon
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/7/1
Y1 - 2024/7/1
N2 - Ammonia (NH3) is gaining attention as a hydrogen carrier due to its high H2 storage capacity and ease of liquefaction at ambient temperatures. The conventional method of ammonia decomposition is thermal cracking through fossil fuel combustion, resulting in significant carbon dioxide (CO2) emissions. Therefore, developing an eco-friendly and highly efficient ammonia decomposition process is important. This study proposed four high-efficiency processes without carbon emissions by improving the induction-heating-based ammonia decomposition process designed in a previous study. The four proposed processes were designed to utilize the H2 discarded as off-gas of the PSA unit in the existing induction-heating-based ammonia decomposition process. The proposed processes incorporate various unit components, including a proton exchange membrane fuel cell (PEMFC), solid oxide fuel cell (SOFC), burner, and palladium (Pd) membrane. These units were integrated with the PSA outlet to achieve enhanced thermodynamic efficiency compared with the conventional process without carbon emissions. Energy, exergy, economic, and environmental analyses were conducted to assess the feasibility of each case. Thermodynamic analysis revealed that integrating the Pd membrane yields the highest thermal (78.29 %) and exergy (64.02 %) efficiencies. Integrating a PEMFC exhibits the lowest levelized cost of H2 (6.93 USD/kg H2). Finally, When the four proposed processes are operated with renewable energy, clean hydrogen can be produced at 2.45 to 3.21 kgCO2/kgH2 emission levels. The enhanced processes presented in this study can serve as a blueprint for achieving carbon-free green H2 production at on-site H2 refueling stations.
AB - Ammonia (NH3) is gaining attention as a hydrogen carrier due to its high H2 storage capacity and ease of liquefaction at ambient temperatures. The conventional method of ammonia decomposition is thermal cracking through fossil fuel combustion, resulting in significant carbon dioxide (CO2) emissions. Therefore, developing an eco-friendly and highly efficient ammonia decomposition process is important. This study proposed four high-efficiency processes without carbon emissions by improving the induction-heating-based ammonia decomposition process designed in a previous study. The four proposed processes were designed to utilize the H2 discarded as off-gas of the PSA unit in the existing induction-heating-based ammonia decomposition process. The proposed processes incorporate various unit components, including a proton exchange membrane fuel cell (PEMFC), solid oxide fuel cell (SOFC), burner, and palladium (Pd) membrane. These units were integrated with the PSA outlet to achieve enhanced thermodynamic efficiency compared with the conventional process without carbon emissions. Energy, exergy, economic, and environmental analyses were conducted to assess the feasibility of each case. Thermodynamic analysis revealed that integrating the Pd membrane yields the highest thermal (78.29 %) and exergy (64.02 %) efficiencies. Integrating a PEMFC exhibits the lowest levelized cost of H2 (6.93 USD/kg H2). Finally, When the four proposed processes are operated with renewable energy, clean hydrogen can be produced at 2.45 to 3.21 kgCO2/kgH2 emission levels. The enhanced processes presented in this study can serve as a blueprint for achieving carbon-free green H2 production at on-site H2 refueling stations.
KW - Ammonia decomposition
KW - Green hydrogen
KW - Life-cycle assessment
KW - On-site hydrogen production
KW - Technoeconomic analysis
UR - http://www.scopus.com/inward/record.url?scp=85192297518&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2024.151875
DO - 10.1016/j.cej.2024.151875
M3 - Article
AN - SCOPUS:85192297518
SN - 1385-8947
VL - 491
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 151875
ER -