TY - JOUR
T1 - One-step conversion of syngas to light olefins over bifunctional metal-zeolite catalyst
AU - Du, Ce
AU - Gapu Chizema, Linet
AU - Hondo, Emmerson
AU - Tong, Mingliang
AU - Ma, Qingxiang
AU - Gao, Xinhua
AU - Yang, Ruiqin
AU - Lu, Peng
AU - Tsubaki, Noritatsu
N1 - Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2021/8
Y1 - 2021/8
N2 - Light olefins (C2–C4) are fundamental building blocks for the manufacture of polymers, chemical intermediates, and solvents. In this work, we realized a composite catalyst, comprising MnxZry oxides and SAPO-34 zeolite, which can convert syngas (CO + H2) into light olefins. MnxZry oxide catalysts with different Mn/Zr molar ratios were facilely prepared using the coprecipitation method prior to physical mixing with SAPO-34 zeolite. The redox properties, surface morphology, electronic state, crystal structure, and chemical elemental composition of the catalysts were examined using H2-TPR, SEM, XPS, XRD, and EDS techniques, respectively. Tandem reactions involved activation of CO and subsequent hydrogenation over the metal oxide catalyst, producing methanol and dimethyl ether as the main reaction intermediates, which then migrated onto SAPO-34 zeolite for light olefins synthesis. Effects of temperature, pressure and reactant gas flow rate on CO conversion and light olefins selectivity were investigated in detail. The Mn1Zr2/SAPO-34 catalyst (Mn/Zr ratio of 1:2) attained a CO conversion of 10.8% and light olefins selectivity of 60.7%, at an optimized temperature, pressure and GHSV of 380 °C, 3 MPa and 3000 h−1 respectively. These findings open avenues to exploit other metal oxides with CO activation capabilities for a more efficient syngas conversion and product selectivity.
AB - Light olefins (C2–C4) are fundamental building blocks for the manufacture of polymers, chemical intermediates, and solvents. In this work, we realized a composite catalyst, comprising MnxZry oxides and SAPO-34 zeolite, which can convert syngas (CO + H2) into light olefins. MnxZry oxide catalysts with different Mn/Zr molar ratios were facilely prepared using the coprecipitation method prior to physical mixing with SAPO-34 zeolite. The redox properties, surface morphology, electronic state, crystal structure, and chemical elemental composition of the catalysts were examined using H2-TPR, SEM, XPS, XRD, and EDS techniques, respectively. Tandem reactions involved activation of CO and subsequent hydrogenation over the metal oxide catalyst, producing methanol and dimethyl ether as the main reaction intermediates, which then migrated onto SAPO-34 zeolite for light olefins synthesis. Effects of temperature, pressure and reactant gas flow rate on CO conversion and light olefins selectivity were investigated in detail. The Mn1Zr2/SAPO-34 catalyst (Mn/Zr ratio of 1:2) attained a CO conversion of 10.8% and light olefins selectivity of 60.7%, at an optimized temperature, pressure and GHSV of 380 °C, 3 MPa and 3000 h−1 respectively. These findings open avenues to exploit other metal oxides with CO activation capabilities for a more efficient syngas conversion and product selectivity.
KW - CO activation
KW - Catalyst
KW - C–C coupling
KW - Hydrogenation
KW - Light olefins
KW - Syngas
UR - http://www.scopus.com/inward/record.url?scp=85104391549&partnerID=8YFLogxK
U2 - 10.1016/j.cjche.2020.09.004
DO - 10.1016/j.cjche.2020.09.004
M3 - 学術論文
AN - SCOPUS:85104391549
SN - 1004-9541
VL - 36
SP - 101
EP - 110
JO - Chinese Journal of Chemical Engineering
JF - Chinese Journal of Chemical Engineering
ER -