Natural gas, or methane, is an abundant resource that is unfortunately underutilized due to a lack of efficient technologies that enable its conversion into easily condensable or liquid products amenable to transport. Most natural gas reserves and the associated gas produced in the course of crude oil production at remote locations are classified as stranded, and venting and flaring is a typical method of disposal, resulting in a significant environmental issue as well as a waste of hydrocarbon resource. Natural gas conversion to liquid fuels and chemicals represents a highly desirable goal since North America has some of the largest gas reserves in the world that can serve as a safe and stable source of hydrocarbons.
Production of chemicals and liquid fuels from methane is currently dominated by technologies that rely on generation of synthesis gas as the first step. These technologies, however, have an inherent inefficiency since the breaking of all methane C-H bonds in synthesis gas production has to be substantially reversed in subsequent steps. There are, therefore, intense current research efforts for development of direct methods for methane conversion. Research on catalytic methane activation remains an area of high scientific and industrial significance but the catalytic chemistry of methane activation is currently poorly understood.
This situation will change with an award made to investigators Simon Podkolzin of the Stevens Institute of Technology, New Jersey, and Israel Wachs of Lehigh University, Pennsylvania. The objective of the proposed research is to develop a molecular level model of catalytic methane conversion to liquid fuels and chemicals by zeolite-supported Mo nanostructures. Methane conversion over Mo nanostructures supported on shape selective zeolites offers a promising alternative for selective methane activation. This chemistry was recently reported by a group from Dalian, China. In this process of methane dehydoaromatization, methane can be converted directly in a single step into benzene with a selectivity of 70-80 mol % and conversions exceeding 10 mol %. In contrast to other direct methane activation chemistries, this process has two unique advantages since methane is converted without any additional reactants. First, complete oxidation of methane to carbon oxides is not possible as in the processes employing O2 or H2O addition. This is also advantageous from the safety perspective. Second, natural gas processing can in concept be performed at remote locations since transportation of reagents is not required.
The PIs intend to study the dynamics of active surface sites at the nanoscale under reaction conditions. They will combine the latest developments in molecular spectroscopic characterization techniques (Raman, IR and UV-vis) at the nanoscale under reaction conditions at elevated temperatures with catalyst kinetic testing, kinetic modeling, and quantum-chemical calculations. Advanced time-resolved atomic XANES/EXAFS characterization will be performed in collaboration with Brookhaven National Laboratory.
Results of this program will have transformative effects in nanotechnology and energy research by developing nanomaterials for efficient conversion of natural gas into liquid hydrocarbons and potentially making available large reserves of stranded gas, while addressing the environmental issue of venting and burning of associated gas at remote locations. A broad spectrum of educational outreach projects is an integral part of the program, including research experiences as well as university and K-12 teaching modules on energy research and nanomaterials.
