TY - JOUR
T1 - Foam-Structured NiO-MgO-Al2O3 Nanocomposites Derived from NiMgAl Layered Double Hydroxides In Situ Grown onto Nickel Foam
T2 - A Promising Catalyst for High-Throughput Catalytic Oxymethane Reforming
AU - Chai, Ruijuan
AU - Li, Yakun
AU - Zhang, Qiaofei
AU - Fan, Songyu
AU - Zhang, Zhiqiang
AU - Chen, Pengjing
AU - Zhao, Guofeng
AU - Liu, Ye
AU - Lu, Yong
N1 - Publisher Copyright:
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/1/23
Y1 - 2017/1/23
N2 - Catalytic oxymethane reforming is an effective and efficient route to produce syngas, but the commonly used Ni catalysts suffer from coke deposition, Ni sintering, and heat-transfer limitations. A Ni-foam-structured NiO-MgO-Al2O3 nanocomposite catalyst was developed by thermal decomposition of NiMgAl layered double hydroxides (LDHs) in situ hydrothermally grown onto the Ni-foam. Originating from the lattice orientation effect and topotactic decomposition of the LDH precursor, NiO, MgO, and Al2O3 are highly distributed in the nanocomposite, and thus, this catalyst shows enhanced resistance to coke and sintering. At 700 °C and a gas hourly space velocity of 100 L g−1 h−1, 86.5 % methane conversion and selectivities of 91.8/88.0 % to H2/CO are achieved with stability for at least 200 h. We believe this type of tailoring strategy and the as-obtained materials can open up new opportunities for future applications in other high-throughput and high-temperature reactions.
AB - Catalytic oxymethane reforming is an effective and efficient route to produce syngas, but the commonly used Ni catalysts suffer from coke deposition, Ni sintering, and heat-transfer limitations. A Ni-foam-structured NiO-MgO-Al2O3 nanocomposite catalyst was developed by thermal decomposition of NiMgAl layered double hydroxides (LDHs) in situ hydrothermally grown onto the Ni-foam. Originating from the lattice orientation effect and topotactic decomposition of the LDH precursor, NiO, MgO, and Al2O3 are highly distributed in the nanocomposite, and thus, this catalyst shows enhanced resistance to coke and sintering. At 700 °C and a gas hourly space velocity of 100 L g−1 h−1, 86.5 % methane conversion and selectivities of 91.8/88.0 % to H2/CO are achieved with stability for at least 200 h. We believe this type of tailoring strategy and the as-obtained materials can open up new opportunities for future applications in other high-throughput and high-temperature reactions.
KW - layered compounds
KW - nickel
KW - oxymethane reforming
KW - structured catalysts
KW - syngas
UR - https://www.scopus.com/pages/publications/85007022821
U2 - 10.1002/cctc.201601167
DO - 10.1002/cctc.201601167
M3 - 文章
AN - SCOPUS:85007022821
SN - 1867-3880
VL - 9
SP - 268
EP - 272
JO - ChemCatChem
JF - ChemCatChem
IS - 2
ER -