Publications by authors named "Xiujing Zou"

Highly dispersed Pt nanoparticles (∼2.5 nm) on phosphorus-doped activated coconut shell carbon (Pt/P-ACC) were synthesized by a two-step impregnation route. Pt/P-ACC showed a high activity, chemoselectivity, and reusability toward the hydrogenation of nitrobenzene to -aminophenol, with hydrogen as the reducing agent in sulfuric acid.

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A series of Al-P-O catalysts (Al-P-O) were prepared using a P123-assisted one-pot method at different P/Al molar ratios and used for -methylation of catechol and methanol. The influences of the P/Al molar ratio and P123 addition on catalyst structure and surface acid-base characteristics were investigated in detail. Increasing the P/Al molar ratio more favored crystalline aluminophosphate.

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Green oxidation of 2,2'-hydrazobis-isobutyronitrile (HAIBN) to 2,2'-azobis-isobutyronitrile (AIBN) over a recyclable solid catalyst was a significant challenge. A titanium dioxide-supported chromium oxide (CrOx/TiO2) catalyst was, for the first time, developed for oxidation of HAIBN with hydrogen peroxide and achieved complete conversion of HAIBN with a high (94.8%) yield of AIBN.

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Herein, nanoscale metallic nanoparticle-incorporated ordered mesoporous carbon catalysts activated by nitrogen-doped graphene (NGr) were fabricated an efficient multi-component co-assembly of a phenolic resin, nitrate, acetylacetone, the nitrogen-containing compound 1,10-phenanthroline, and Pluronic F127, followed by carbonization. The obtained well-dispersed nitrogen-doped graphene-activated transition metal nanocatalysts possess a 2-D hexagonally arranged pore structure with a high surface area (∼500 m g) and uniform pore size (∼4.0 nm) and show excellent activity for the selective hydrogenation-reduction of substituted nitroarenes to anilines in an environmentally friendly aqueous solution.

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Mesoporous γ-alumina (γ-MA)-supported cobalt oxides (CoO) with large surface areas and narrow pore size distributions were first prepared through one-pot hydrolysis of metal nitrates. The obtained CoO/γ-MA materials were impregnated with a water-ethanol solution of 1,10-phenanthroline, followed by treatment at 700 °C in N atmosphere, generating Co-NC/γ-MA catalysts containing N-doped graphitic carbon (NC). The Co-NC/γ-MA catalysts maintained the mesoporous structure of γ-MA, and CoO was reduced to metallic Co nanoparticles highly dispersed in the γ-MA frameworks.

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Direct synthesis of metal/carbon nanocomposites with ordered mesoporous frameworks has attracted increasing interest in various applications including catalysis, optics, and electronics. Herein, we demonstrate a simple one-pot co-assembly route to synthesize Ru/carbon composites by using resol, ruthenium chloride, and Pluronic F127 as a template with the assistance of 8-hydroxyquinoline. 8-Hydroxyquinoline exerts a significant influence on the mesostructure ordering and specific surface area of the Ru/carbon composites.

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The synthesis of mesoporous SBA-15 coated with the preformed precursor of microporous aluminophosphate (AlPO) has been reported. The physicochemical properties of the coated samples were investigated by using XRD, FT-IR, N(2)-adsorption, ICP, (29)Si MAS NMR, NH(3)-TPD and CO(2)-TPD. The characterization results suggest that the nanometer-scaled zeolite units are present on the wall surface of SBA-15, thus bringing the weak acid-base characteristics to the resulting mesoporous materials, and that the acid-base properties of these materials can be modified by the aging treatment in glycol.

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Amorphous mesoporous aluminophosphates (AlPO) with P/Al molar ratio in the range 0.8-1.15 are synthesized by using the citric acid (CA) route and are systematically characterized using N(2)-adsorption, XRD, SEM, solid-state CP-MAS NMR, FT-IR, TG-DTA, CO(2)-TPD, and NH(3)-TPD.

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