Hydrogen generation from the hydrolysis of ammonia borane using cobalt-nickel-phosphorus (Co-Ni-P) catalyst supported on Pd-activated TiO2 by electroless deposition

Date

2011-01-01

Author

Rakap, Murat
Kalu, Egwu Eric
Özkar, Saim

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Catalytically active, low-cost, and reusable transition metal catalysts are desired to develop on-demand hydrogen generation system for practical onboard applications. By using electroless deposition method, we have prepared the Pd-activated TiO2-supported Co-Ni-P ternary alloy catalyst (Co-Ni-P/Pd-TiO2) that can effectively promote the hydrogen release from ammonia-borane aqueous solution. Co-Ni-P/Pd-TiO2 catalysts are stable enough to be isolated as solid materials and characterized by XRD, SEM, and EDX. They are isolable, redispersible and reusable as an active catalyst in the hydrolysis of AB. The reported work also includes the full experimental details for the collection of a wealth of kinetic data to determine the activation energy (E-a = 54.9 kJ mol(-1)) and effects of the amount of catalyst, amount of substrate, and temperature on the rate for the catalytic hydrolysis of AB. Maximum H-2 generation rate of similar to 60 mL H-2 min(-1) (g catalyst)(-1) and similar to 400 mL H-2 min(-1) (g catalyst)(-1) was measured by the hydrolysis of AB at 25 degrees C and 55 degrees C, respectively. (C) 2010 Professor T. Nejat Veziroglu. Published by Elsevier Ltd. All rights reserved.

Subject Keywords

Fuel Technology, Renewable Energy, Sustainability and the Environment, Energy Engineering and Power Technology, Condensed Matter Physics

URI

https://hdl.handle.net/11511/62797

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY

DOI

https://doi.org/10.1016/j.ijhydene.2010.09.027

Collections

Department of Chemistry, Article

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Citation Formats

M. Rakap, E. E. Kalu, and S. Özkar, “Hydrogen generation from the hydrolysis of ammonia borane using cobalt-nickel-phosphorus (Co-Ni-P) catalyst supported on Pd-activated TiO2 by electroless deposition,” INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, pp. 254–261, 2011, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/62797.