Related Experiment Video
Updated: Jan 15, 2026

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
Transition-Metal-Free Zeolite Composites for Tandem Catalytic Conversion of Methane to Light Olefins
Peipei Xiao1, Hiroto Toyoda1, Yuqin Sun1
1Institute of Integrated Research, Institute of Science Tokyo, 4259 Nagatsuta, Midori-ku, Yokohama, 226-8501, Japan.
Abstract:
The methanol-to-olefins (MTO) reaction is considered one of the most important reactions in C1 chemistry, offering a route to produce basic petrochemicals from non-oil resources such as natural gas and coal. Direct conversion of methane, the primary component of natural gas, to olefins via methanol as an intermediate is of significant industrial interest. Recent studies demonstrate that methanol can be efficiently synthesized from methane using transition-metal-free aluminosilicate Ferrierite (FER) zeolite with nitrous oxide (N2O) as the oxidant. Herein, a tandem catalytic system based on the composite FER and one more acidic zeolite is reported to achieve continuous conversion of methane to olefins. The topology and acidity of acidic zeolites critically influenced product distribution and hydrocarbon formation rates. When small-pore zeolites are used as acidic zeolites, complete conversion of methanol to olefins is successfully achieved. Reaction conditions for methane-to-olefins conversion are optimized using silicoaluminophosphate (SAPO-34) as a representative acidic zeolite. The mass ratio of FER to SAPO-34 determined catalytic performance, with conversion of methane to light olefins achieving thermodynamic feasibility at 325-400 °C. Enhanced intimacy between FER and SAPO-34 particles promoted methane (CH4) conversion. This work establishes an efficient strategy for high-selectivity light olefin production from methane over integrated transition-metal-free zeolite catalysts.
More Related Videos
Related Concept Videos
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.

