TY - JOUR
T1 - Oxidative coupling of methane using catalysts synthesized by solution combustion method
T2 - Catalyst optimization and kinetic studies
AU - Ghose, Ranjita
AU - Hwang, Hyun Tae
AU - Varma, Arvind
PY - 2014/2/22
Y1 - 2014/2/22
N2 - Abstract The Na2WO4-Mn/SiO2 catalyst has shown promise for oxidative coupling of methane (OCM). Our prior work demonstrates that 10%Na2WO4-5%Mn/SiO2 prepared by solution combustion synthesis (SCS) exhibits good performance in terms of C2 yield and ethylene to ethane ratio. In this work, we use SCS for preparation of several modified Na2WO4-Mn/SiO2 catalysts for OCM. The catalyst composition was optimized by addition of different metals and Si precursor used. The optimized catalyst (5%La-10%Na 2WO4-5%Mn/SiO2, using tetraethoxysilane as the Si precursor) showed the best performance for OCM, with C2 yield 27% and ethylene/ethane ratio 3.6 under optimized operating conditions, both values are among the highest reported in the literature. Kinetic studies for this catalyst indicated that methane conversion was first-order in methane and half-order in oxygen, implying that methane activation is likely to be rate-limiting and oxygen adsorption is dissociative. The formation rates of primary products (C2H6, CO and CO2) could be well described by the reaction scheme proposed in a prior work.
AB - Abstract The Na2WO4-Mn/SiO2 catalyst has shown promise for oxidative coupling of methane (OCM). Our prior work demonstrates that 10%Na2WO4-5%Mn/SiO2 prepared by solution combustion synthesis (SCS) exhibits good performance in terms of C2 yield and ethylene to ethane ratio. In this work, we use SCS for preparation of several modified Na2WO4-Mn/SiO2 catalysts for OCM. The catalyst composition was optimized by addition of different metals and Si precursor used. The optimized catalyst (5%La-10%Na 2WO4-5%Mn/SiO2, using tetraethoxysilane as the Si precursor) showed the best performance for OCM, with C2 yield 27% and ethylene/ethane ratio 3.6 under optimized operating conditions, both values are among the highest reported in the literature. Kinetic studies for this catalyst indicated that methane conversion was first-order in methane and half-order in oxygen, implying that methane activation is likely to be rate-limiting and oxygen adsorption is dissociative. The formation rates of primary products (C2H6, CO and CO2) could be well described by the reaction scheme proposed in a prior work.
KW - Ethylene
KW - Kinetics
KW - Methane
KW - Mixed oxide catalyst
KW - Oxidative coupling of methane
KW - Solution combustion synthesis (SCS)
UR - http://www.scopus.com/inward/record.url?scp=84891621534&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84891621534&partnerID=8YFLogxK
U2 - 10.1016/j.apcata.2013.12.004
DO - 10.1016/j.apcata.2013.12.004
M3 - Article
AN - SCOPUS:84891621534
SN - 0926-860X
VL - 472
SP - 39
EP - 46
JO - Applied Catalysis A: General
JF - Applied Catalysis A: General
ER -