Mesoporous Matrix Encapsulation for the Synthesis of Monodisperse Pd5P2 Nanoparticle Hydrodesulfurization Catalysts
Source abstract
Abstract
The synthesis of monodisperse 5-10 nm Pd5P2 catalytic particles by encapsulation in a mesoporous silica network, along with preliminary data on hydrodesulfurization (HDS) activity, is reported. Precursor Pd-P amorphous nanoparticles are prepared by solution-phase reaction of palladium(II) acetylacetonate with trioctylphosphine at temperatures up to 300 °C. Direct crystallization of Pd5P2 in solution by increasing the temperature to 360 °C leads to sintering, but particle size can be maintained during the transformation by encapsulation of the amorphous Pd-P particles in a mesoporous silica shell, followed by treatment of the solid at 500 °C under a reducing atmosphere, yielding Pd5P2@mSiO2. The resultant materials exhibit high BET surface areas (>1000 m(2)/g) and an average pore size of 3.7 nm. Access to the catalyst surface is demonstrated by dibenzodithiophene (DBT) HDS testing. Pd5P2@mSiO2 shows a consistent increase in HDS activity as a function of temperature, with DBT conversion approaching 60% at 402 °C. The ability to control particle size, phase, and sintering is expected to enable the fundamental catalytic attributes that underscore activity in Pd5P2 to be assessed.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Catalysis and Hydrodesulfurization Studies · Nanomaterials for catalytic reactions · Catalytic Processes in Materials Science
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Wayne State University, Detroit, Michigan 48202, United States
Department of Chemistry, Western Washington University, Bellingham, Washington 98225-9150, United States
References (24)
Show source-provided references
1. Pawelec B. · Cat. Rev.–Sci. Eng. · 2011 · 1 · 23
2. Bej S. K. · Energy Fuels · 2004 · 18 · 122710.1021/ef030179+ ↗
3. Schulz H. · Fuel Process. Technol. · 1999 · 61 · 510.1016/S0378-3820(99)00028-4 ↗
4. Whitehurst D. D. · Catal. Today · 1998 · 45 · 29910.1016/S0920-5861(98)00234-X ↗
5. Zepeda T. A. · Appl. Catal., B · 2007 · 71 · 22310.1016/j.apcatb.2006.09.011 ↗
6. Qian E. W. · J. Catal. · 2004 · 221 · 29410.1016/S0021-9517(03)00280-X ↗
7. Röthlisberger A. · J. Catal. · 2005 · 235 · 22910.1016/j.jcat.2005.08.007 ↗
8. Niquille-Röthlisberger A. · J. Catal. · 2006 · 242 · 20710.1016/j.jcat.2006.06.009 ↗
9. Kuhn, J. N.InCatalysis;Spivey, J. M.; Dooley, K. M, Eds.Royal Society of Chemistry: London, 2011; Vol.23, p96–138.
10. Hayes J. R. · J. Catal. · 2010 · 276 · 24910.1016/j.jcat.2010.09.013 ↗
11. Kanda Y. · J. Jpn. Pet. Inst. · 2012 · 55 · 10810.1627/jpi.55.108 ↗
12. Kanda Y. · Appl. Catal., A · 2010 · 386 · 17110.1016/j.apcata.2010.07.045 ↗
13. Bowker R. H. · Top. Catal. · 2012 · 55 · 99910.1007/s11244-012-9887-y ↗
14. Guan Q. · Catal. Commun. · 2011 · 14 · 11410.1016/j.catcom.2011.08.005 ↗
15. Prins R. · Catal. Lett. · 2012 · 142 · 141310.1007/s10562-012-0929-7 ↗
16. Henkes A. E. · J. Am. Chem. Soc. · 2007 · 129 · 189610.1021/ja068502l ↗
17. Carenco S. · Chem. Mater. · 2012 · 24 · 413410.1021/cm3022243 ↗
18. Wang J. · Chem. Mater. · 2009 · 21 · 446210.1021/cm901073k ↗
19. Muthuswamy E. · ACS Nano · 2011 · 5 · 240210.1021/nn1033357 ↗
20. Moreau L. M. · Nano Lett. · 2012 · 12 · 453010.1021/nl301642g ↗
21. Layan Savithra G. H. · Chem. Mater. · 2013 · 25 · 82510.1021/cm302680j ↗
22. Wang J. · Chem.—Eur. J. · 2010 · 16 · 791610.1002/chem.200902151 ↗
23. Wang Z. · Chem. Asian. J. · 2009 · 4 · 179410.1002/asia.200900232 ↗
24. Zafiropoulou I. · J. Phys. Chem. C. · 2010 · 114 · 758210.1021/jp910160g ↗