TY - JOUR
T1 - Phosphorus promoted HZSM-5 zeolites for the coupling transformation of methanol with 1-butene to propylene
AU - Tang, Xiao Hua
AU - Liu, Rui Qiang
AU - Tian, Hai Feng
AU - Li, Hui
AU - Zha, Fei
AU - Chang, Yue
N1 - Publisher Copyright:
© 2021, Canadian Science Publishing. All rights reserved.
PY - 2021
Y1 - 2021
N2 - Phosphorus promoted HZSM-5 zeolites (P-HZSM-5) were prepared by synthetic methods of incipient wetness impregnation and in situ synthesis, respectively. This was characterized by the means of powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller method (BET), thermogravimetry (TG), and NH3-TPD. The P-HZSM-5 zeolite prepared by incipient wetness impregnation has a large specific surface area and pore size, and the weak acidity is remarkably increased. The catalytic activity of P-HZSM-5 for the coupling transformation of methanol with 1-butene to propylene was investigated. Under the reaction conditions of temperature at 550 °C, pressure at 0.4 MPa, space velocity at 1800 mL/(gcat h), and mole ratio of CH3OH/C4H8 at 1:1, the conversion of C4H8 can reach to 75.8%, and the selectivity and yield of propylene are 42.2% and 31.9%, respectively.
AB - Phosphorus promoted HZSM-5 zeolites (P-HZSM-5) were prepared by synthetic methods of incipient wetness impregnation and in situ synthesis, respectively. This was characterized by the means of powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller method (BET), thermogravimetry (TG), and NH3-TPD. The P-HZSM-5 zeolite prepared by incipient wetness impregnation has a large specific surface area and pore size, and the weak acidity is remarkably increased. The catalytic activity of P-HZSM-5 for the coupling transformation of methanol with 1-butene to propylene was investigated. Under the reaction conditions of temperature at 550 °C, pressure at 0.4 MPa, space velocity at 1800 mL/(gcat h), and mole ratio of CH3OH/C4H8 at 1:1, the conversion of C4H8 can reach to 75.8%, and the selectivity and yield of propylene are 42.2% and 31.9%, respectively.
KW - 1-butene
KW - Coupling transformation
KW - Methanol
KW - Phosphorus promoted HZSM-5
KW - Propylene
UR - http://www.scopus.com/inward/record.url?scp=85105435245&partnerID=8YFLogxK
U2 - 10.1139/cjc-2020-0316
DO - 10.1139/cjc-2020-0316
M3 - Article
AN - SCOPUS:85105435245
SN - 0008-4042
VL - 99
SP - 474
EP - 481
JO - Canadian Journal of Chemistry
JF - Canadian Journal of Chemistry
IS - 5
ER -