TY - JOUR
T1 - ZnO-ZnCr2O4 composite prepared by a glycine nitrate process method and applied for hydrogen production by steam reforming of methanol
AU - Yu, Chung Lun
AU - Sakthinathan, Subramanian
AU - Lai, Guan Ting
AU - Lin, Chia Cheng
AU - Chiu, Te Wei
AU - Liu, Ming Che
N1 - Funding Information:
This work was supported by the Ministry of Science and Technology of Taiwan (MOST 108-2221-E-027-056, MOST 109-2221-E-027-068, MOST 109-2221-E-027-059, and MOST 109-2113-M-027-001-MY3). This work was supported by the National Science and Technology Council of Taiwan (NSTC 111-2221-E-027-104). This work was supported by University System of Taipei Joint Research Program (USTP-NTUT-TMU-111-01). The authors appreciate the Precision Research and Analysis Centre of National Taipei University of Technology (NTUT) for providing the measurement facilities.
Publisher Copyright:
© 2022 The Royal Society of Chemistry.
PY - 2022/8
Y1 - 2022/8
N2 - To address climate change, the energy crisis, and global warming, hydrogen (H2) can be used as a potential energy carrier because it is clean, non-toxic and efficient. Today, the mainstream industrial method of H2 generation is steam reforming of methanol (SRM). In this process, a zinc-based commercial catalyst is usually used. In this work, a ZnO-ZnCr2O4 catalyst was successfully synthesised by the glycine nitrate process (GNP) and developed for use in H2 production by SRM. The specific surface area, porous structure and reaction sites of the zinc-based catalyst were effectively increased by the preparation method. The as-combusted ZnO-ZnCr2O4 composite catalyst had a highly porous structure due to the gas released during the GNP reaction process. Moreover, according to the ZnO distribution and different G/N ratios, the specific surface area (SBET) of the as-combusted ZnO-ZnCr2O4 catalyst varied from 29 m2 g−1 to 46 m2 g−1. The ZnO-ZnCr2O4 composite catalyst (G/N 1.7) exhibited the highest hydrogen production, 4814 ml STP min−1 g-cat−1, at a reaction temperature of 450 °C without activation treatment. After activation, the ZnO-ZnCr2O4 composite catalyst achieved hydrogen production of 6299 ml STP min−1 g-cat−1 at a reaction temperature of 500 °C. The hydrogen production performance of the ZnO-ZnCr2O4 composite powder was improved by the uniform addition of ZnO to ZnCr2O4. Based on the performance, this ZnO-ZnCr2O4 composite catalyst has great potential to have industrial and economic impact due to its high efficiency in hydrogen production.
AB - To address climate change, the energy crisis, and global warming, hydrogen (H2) can be used as a potential energy carrier because it is clean, non-toxic and efficient. Today, the mainstream industrial method of H2 generation is steam reforming of methanol (SRM). In this process, a zinc-based commercial catalyst is usually used. In this work, a ZnO-ZnCr2O4 catalyst was successfully synthesised by the glycine nitrate process (GNP) and developed for use in H2 production by SRM. The specific surface area, porous structure and reaction sites of the zinc-based catalyst were effectively increased by the preparation method. The as-combusted ZnO-ZnCr2O4 composite catalyst had a highly porous structure due to the gas released during the GNP reaction process. Moreover, according to the ZnO distribution and different G/N ratios, the specific surface area (SBET) of the as-combusted ZnO-ZnCr2O4 catalyst varied from 29 m2 g−1 to 46 m2 g−1. The ZnO-ZnCr2O4 composite catalyst (G/N 1.7) exhibited the highest hydrogen production, 4814 ml STP min−1 g-cat−1, at a reaction temperature of 450 °C without activation treatment. After activation, the ZnO-ZnCr2O4 composite catalyst achieved hydrogen production of 6299 ml STP min−1 g-cat−1 at a reaction temperature of 500 °C. The hydrogen production performance of the ZnO-ZnCr2O4 composite powder was improved by the uniform addition of ZnO to ZnCr2O4. Based on the performance, this ZnO-ZnCr2O4 composite catalyst has great potential to have industrial and economic impact due to its high efficiency in hydrogen production.
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U2 - 10.1039/d2ra03383f
DO - 10.1039/d2ra03383f
M3 - Article
AN - SCOPUS:85137406423
SN - 2046-2069
VL - 12
SP - 22097
EP - 22107
JO - RSC Advances
JF - RSC Advances
IS - 34
ER -