Consolidation of metal oxide nanocrystals. Reactive pellets with controllable pore structure that represent a new family of porous, inorganic materials
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Richards, R
Li, WF
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机构:Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
Li, WF
Decker, S
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机构:Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
Decker, S
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Davidson, C
Koper, O
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机构:Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
Koper, O
Zaikovski, V
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机构:Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
Zaikovski, V
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Volodin, A
Rieker, T
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机构:Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
Rieker, T
Klabunde, KJ
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Kansas State Univ, Dept Chem, Manhattan, KS 66506 USAKansas State Univ, Dept Chem, Manhattan, KS 66506 USA
Klabunde, KJ
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[1] Kansas State Univ, Dept Chem, Manhattan, KS 66506 USA
[2] Nantek Inc, Manhattan, KS 66502 USA
[3] Boreskov Inst Catalysis, Novosibirsk 630090, Russia
[4] Univ New Mexico, Dept Chem & Nucl Engn, Albuquerque, NM 87131 USA
Nanocrystals of MgO (4 nm) exist as polyhedral structures with high surface concentrations of edge/corner sites. In powder form the crystallites weakly agglomerate into porous weblike structures of approximately 1400 nm according to small-angle X-ray scattering. Upon consolidation of these fine powders under pressure, pellets can be readily prepared that maintain their high surface areas, and small crystallite sizes. In addition, large pore volumes and pore size openings can be controllably decreased with pelletization pressure increase. The pellets retain their voracious adsorbent affinities and capacities for a wide variety of organic molecules and acid gases. Quantitative measurements on the adsorption of a series of alcohols vs pelletization pressure reveal a pattern of molecular size selectivity.