Early Transition Metal Carbide and Nitride Supported Catalysts for Ammonia Synthesis

Zixuan Wang*, Levi T. Thompson
University of Michigan, United States

NH3 Fuel Conference, Minneapolis, November 2, 2017
AIChE Annual Meeting, Topical Conference: NH3 Energy+

ABSTRACT

More than 180 million tons of NH3 are produced annual via the Haber-Bosch process which converts N2 and H2 at high temperatures (400 – 500°C) and pressures (150 – 300 bars). Ammonia synthesis also accounts for 1-2% of global energy consumption.1 The development of higher activity catalysts that can operate under less severe conditions would enhance the economics associated with and sustainability of NH3 synthesis.

Research described in this paper investigates the performance of transition metal carbide and nitride supported metals for NH3 synthesis. Previously, Mo2C and Mo2N have been reported to be more active than Ru-based catalysts, but slightly less active than the doubly-promoted Fe catalyst typically used in industrial processes.2 To enhance the performance of the bulk carbides and nitrides, we introduced metals including Fe and Ru. While carbide and nitride supported metal catalysts have typically been produced using the passivated supports, the method that we used allows for direct interaction between the metal and support material.

The Mo2C and Mo2N supports were synthesized via a temperature program reaction method. To synthesize the Mo2C, ammonium paramolybdate was reacted with flowing H2 then a 15% CH4/H2 mixture. To synthesize the Mo2N, ammonium paramolybdate was reacted with flowing NH3. The resulting support materials were either passivated with 1% O2/He, or a metal support (e.g. Fe and Ru) was introduced via dry impregnation, followed by reduction and passivation. The materials were evaluated for NH3 synthesis at 14.7 psi and 400-500 °C using a stoichiometric mixture of N2 and H2, and characterized using techniques include X-ray diffraction and elemental analysis.

X-ray diffraction patterns for the Mo2C contained peaks characteristic for α-MoC1-x and β-Mo2C, while patterns for the Mo2N indicated the presence of γ-Mo2N. Surface areas for the Mo2C and Mo2N supports were 113 and 85 m2/g, respectively. The addition of metal supports caused a significant reduction in the surface area. For example, the surface area for the Fe/Mo2C catalyst was 30 m2/g. Nevertheless, all of the catalysts were highly active for NH3 synthesis. Production rates for Mo2C, Mo2N, and Fe/Mo2C were 120 μmol/hr g, 130 μmol/hr g, and 60 μmol/hr g, respectively. The specific activity for the Fe/Mo2C catalyst was the highest (1.49 μmol/hr m2) among the catalysts evaluated and is higher than values previously reported in the literature.3 These and other results will be described in the presentation.

References:
[1] S. Back;Y. Jung, Phys. Chem. Chem. Phys., 2016, 18, 9161.
[2] S. T. Oyama, Catal. Today, 1992, 15, 179.
[3] R. Kojima, K. Aika, Appl. Catal. A: General 2001, 219, 141.

Read the abstract at the AIChE website.

DOWNLOAD

Download this presentation [PDF, 5MB].

LINKS

Levi T. Thompson, University of Michigan
Learn more about the NH3 Fuel Conference 2017

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