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Libo Qin

Researcher at Beijing University of Chemical Technology

Publications -  15
Citations -  240

Libo Qin is an academic researcher from Beijing University of Chemical Technology. The author has contributed to research in topics: Catalysis & Mesoporous material. The author has an hindex of 7, co-authored 15 publications receiving 166 citations.

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Highly Dispersed HKUST-1 on Milimeter-Sized Mesoporous γ-Al2O3 Beads for Highly Effective Adsorptive Desulfurization

TL;DR: Hong et al. as mentioned in this paper impregnated a millimeter-sized mesoporous γ-Al2O3 beads under hydrothermal conditions, resulting in formation of a composite material HKUST-1@γ-Al 2O3 that features high specific surface area, remarkable enhanced mechanical strength, chemical and thermal stability, and low cost.
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Confinement of microporous MOF-74(Ni) within mesoporous γ-Al2O3 beads for excellent ultra-deep and selective adsorptive desulfurization performance

TL;DR: In this paper, the microporous MOF-74(Ni) was impregnated on mesoporous γ-Al2O3 beads leading to successful formation of a hierarchical multiporous composite, which was applied for ultra-deep adsorptive desulfurization.
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Phosphotungstic acid immobilized on amino functionalized spherical millimeter-sized mesoporous γ-Al2O3 bead and its superior performance in oxidative desulfurization of dibenzothiophene

TL;DR: In this article, a composite material HPW/NH 2 -Al 2 O 3 was successfully prepared by immobilization of phosphotungstic acid H 3 PW 12 O 40 (HPW) on the surface of amino functionalized spherical millimeter-sized mesoporous γ-Al 2O 3 beads.
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In situ formation of a multiporous MOF(Al)@γ-AlOOH composite material: A versatile adsorbent for both N- and S-heterocyclic fuel contaminants with high selectivity

TL;DR: In this article, an in situ green synthetic approach for the formation of a multiporous (mesoporous) composite, Al(OH)(1,4-NDC)@γ-AlOOH, via a direct hydrothermal reaction between 1, 4-H2NDC and millimeter-sized porous γ-Al2O3 beads was reported.
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Enhanced adsorptive desulfurization by iso-structural amino bearing IRMOF-3 and IRMOF-3@Al2O3versus MOF-5 and MOF-5@Al2O3 revealing the predominant role of hydrogen bonding.

TL;DR: The kinetics and thermodynamic parameters indicate that the adsorption process is spontaneous and endothermic, and the increase in entropy is the primary driving force for the desulfurization.