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A novel boronic acid functionalized mesoporous silica, which holds the attractive features of high surface area and large accessible porosity, was developed to enrich glycopeptides. This is the first time that mesoporous material has been introduced into glycoproteome. In comparison to direct (traditional) analysis, this novel method enabled 2 orders of magnitude improvement in the detection limit of glycopeptides. The unbiased nature of organo-boronic acid groups also made this method applicable to all kinds of glycopeptides regardless of their sizes, structures, and hydrophilicities. [ABSTRACT FROM AUTHOR]

A novel boronic acid functionalized mesoporous silica, which holds the attractive features of high surface area and large accessible porosity, was developed to enrich glycopeptides. This is the first time that mesoporous material has been introduced into glycoproteome. In comparison to direct (traditional) analysis, this novel method enabled 2 orders of magnitude improvement in the detection limit of glycopeptides. The unbiased nature of organo-boronic acid groups also made this method applicable to all kinds of glycopeptides regardless of their sizes, structures, and hydrophilicities. [ABSTRACT FROM AUTHOR]

HKUST-1 was impregnated effectively on millimeter-sized mesoporous γ-Al2O3 beads under hydrothermal conditions, resulting in formation of a composite material HKUST-1@γ-Al2O3 that features high specific surface area, remarkable enhanced mechanical strength, chemical and thermal stability, and low cost. The composite material exhibited excellent performance with the adsorptive desulfurization capacity of 59.7 mg S/g MOF (versus 49.1 mg S/g MOF for bare HKUST-1) for a model oil composed of dibenzothiophene (with the initial S-content being 1000 ppmwS) and n-octane. Experimental results also revealed that HKUST-1@γ-Al2O3 could reduce 35 ppmwS sulfur content of the model oil lower than 9.6 ppmwS at a ratio of HKUST-1@γ-Al2O3 to oil over 30 wt %, indicating effectiveness for deep adsorptive desulfurization. The Gibbs free energy for DBT adsorption by HKUST-1@γ-Al2O3 was found smaller than that by HKUST-1 due to efficient utilization of active centers, shorter diffusion channels and larger specific surface area of nanosized HKUST-1 particles formed under confined environment of γ-Al2O3 channels/pores. Remarkably, the used HKUST-1@γ-Al2O3 beads can easily be regenerated by acetone washing and the adsorptive desulfurization capacity just slightly decreased after experiencing five recycles. The results indicate that the as-synthesized HKUST-1@γ-Al2O3 beads have great potential as an adsorbent for adsorptive desulfurization in practical applications. [ABSTRACT FROM AUTHOR]

Uniform oxide deposition on graphene to form a sandwich-like configuration is a well-known challenge mainly due to their large lattice mismatches and poor affinities. Herein, we report a general strategy to synthesize uniform mesoporous TiO2/graphene/mesoporous TiO2 sandwich-like nanosheets (denoted as G@mTiO2), which cannot be achieved by conventional one-pot synthetic methods. We show that by rational control of hydrolysis and condensation of Ti precursors in a slow way, GO sheets can be conformably coated by amorphous TiO2 shells, which then can be facilely transformed into the well-defined G@mTiO2 nanosheets by annealing. This amorphous-to-crystalline strategy conveniently allows bypassing strain fields that would inevitably arise if direct growth of mesoporous anatase shells on graphene. As distinct from the most common structures of graphene-based composites (mixed, wrapped, or anchored models), the resultant materials display a uniform sandwich-like configuration: few-layer graphene conformably encapsulated by mesoporous TiO2 shells. This new G@mTiO2 nanosheet exhibits ultrathin nature (~34 nm), small size and high crystalline nanocrystals (~6 nm), high surface areas (~252 m²/g) and uniform mesopores (~3.4 nm). We further show that the thickness of mesoporous TiO2 shells can be facilely adjusted as desired by controlling the ammonia content, and this facile strategy can be easily extended to design other oxide/graphene/oxide sandwich-like materials. More importantly, we showcase the benefits of the resultant G@mTiO2 nanosheets as anodes in lithium ion batteries: they deliver an extra high capacity, an excellent high-rate capability, and long cycle life. [ABSTRACT FROM AUTHOR]