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Results for “ADSORPTION”
Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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Role of defects and metal coordination on adsorption of acid gases in MOFs and metal oxides: An in situ IR spectroscopic study
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Significantly increasing porosity of mesoporous carbon by NaNH 2 activation for enhanced CO 2 adsorption
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Influence of brønsted-acid and cation-exchange sites on ethene adsorption in ZSM-5
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Lifting of the Au(100) surface reconstruction by Pt, Cr, Fe, and Cu adsorption
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Coverage-dependent adsorption of small gas molecules on black phosphorene: a DFT study
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Lead immobilization by phosphate in the presence of iron oxides: Adsorption versus precipitation
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Template-Assisted, Seed-Mediated Synthesis of Hierarchically Mesoporous Core–Shell UiO-66: Enhancing Adsorption Capacity and Catalytic Activity through Iterative Growth
A hierarchically mesoporous (HM) UiO-66-F 4 shell with ~8 nm mesopores can be iteratively grown on top of UiO-66 nanoparticle (NP) seeds over several cycles templated by Pluronic F-127 micelles. Presumably, the Pluronic micelles that were formed in water can surround UiO-66 NPs to facilitate the overgrowth of an HM-UiO-66-F 4 shell in the presence of Zr IV precursors and BDC-F 4 linkers. The UiO-66 NP seeds play an important role in directing the continuous growth of the HM-UiO-66-F 4 shell, as only a nonporous phase was obtained in their absence. Furthermore, this template-assisted, seed-mediated method can be extended to produce other UiO-66-X (X = (OH) 2 , (COOH) 2 , etc.) shells, demonstrating its generality for the UiO-66 family of metal–organic frameworks. Notably, the incorporation of mesopores into the thrice-overgrown UiO-66@HM|3rd-UiO-66-F 4 materials leads to impressive enhancements in the per-mass uptake capacity of Direct Blue 86, a large anionic dye: 320% better than the parent UiO-66 seeds and 150% better than that for a [UiO-66 + UiO-66-F 4 ] physical mixture at the same mass proportion. Similar enhancements were also observed in the catalyzed oxidation of thioanisole.
Adsorption of a catalytically accessible polyoxometalate in a mesoporous channel-type metal–organic framework
A Keggin-type polyoxometalate (H 3 PW 12 O 40 ) was incorporated into a mesoporous Zr-based MOF (NU-1000) via an impregnation method in aqueous media, resulting in the hybrid material, PW 12 @NU-1000. The POM@MOF composite was characterized by a suite of physical methods, indicating the retention of crystallinity and high porosity of the parent MOF. The hybrid material was also stable to leaching in aqueous media at varying pH. Lastly, the material was tested as a heterogeneous catalyst for the oxidation of 2-chloroethyl ethyl sulfide using hydrogen peroxide as the oxidant. PW 12 @NU-1000 was shown to have a higher catalytic activity than either of the individual constituents alone.
Theoretical Study of EMIM + Adsorption on Silver Electrode Surfaces
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