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Nanorod-like phosphorus-doped ordered mesoporous γ-alumina (OMA), which has abundant ordered pore channels in the nanorods, was rapidly synthesized through a modified sol–gel strategy without use of any mineral acids. Highly dispersed Pd-based catalysts were synthesized by taking as-obtained phosphorus-doped OMA materials as carriers for methane combustion. The crystallization temperature of γ-Al2O3 was increased by phosphorus doping. The surface acidity properties of γ-Al2O3 were modified upon phosphorus incorporation, which had a significant effect on catalyst activities, and this influence was much more conspicuous for the supports calcined at high temperature. The incorporation of phosphorus adjusted the distribution of palladium active species and the reducibility of catalysts, synergistically affecting the low-temperature catalytic performance. Pd/6P-OMA catalyst demonstrated enhanced low-temperature catalytic properties and stability in the 13-cycle stability and long-term stability tests. During the reaction cycles, the total CH4 conversion temperature for Pd/6P-OMA catalyst was as low as 345 °C, which could be reduced to 321 °C via hydrogen reduction treatment. In comparison with the catalyst without dopant, the Pd/6P-OMA catalyst also exhibited higher hydrothermal stability in the presence of excess water vapor in the feed.

CeO2-based catalysts are potentially suitable for H2S-selective oxidation, but their practical application is limited due to the problem of sulfate formation. Herein, we report a facile citric acid-assisted hydrothermal process for the fabrication of porous Fe-doped CeO2 with flower-like morphology that can drastically promote the catalytic activities of CeO2 with high durability. Among the synthesized catalysts, the one with well-defined (110) and (100) planes is highly active for H2S-selective oxidation with H2S conversion and sulfur selectivity of almost 100% at 220 °C, superior to most of the reported Ce-based catalysts. Meanwhile, outstanding catalytic stability is achieved because the presence of Fe ions alleviates ceria deactivation due to sulfation. The results of systematic investigation prove that the doping of Fe not only raises the density of oxygen vacancies but also promotes the redox ability and oxygen activity of the catalyst. We conducted in situ DRIFTS (diffuse reflection infrared Fourier transform spectroscopy) experiments and density functional theory (DFT) calculations to disclose the reaction mechanism of H2S oxidation. The derived insights are important for the design of efficient ceria-related catalysts for practical applications.

A series of graphitic carbon nitride (CN) in the form of nanosheets with porous structure have been prepared through thermal treatment of bulk CN in air. Compared with the bulk counterpart, the as-generated holey CN nanosheets are larger in specific surface area. Endowed with more active sites and enhanced mass transport ability, the latter display catalytic performance substantially superior to the former, exhibiting higher H2S conversion and S selectivity in the oxidation of H2S to S. Moreover, the CN nanosheets show much better durability than traditional catalysts. It is envisaged that the strategy is a general technique that can be extended to produce porous CN nanosheets from other nitrogen-rich precursors, as well as to prepare other 2D carbon-based materials for potential applications.

An efficient protocol for the synthesis of hydroxyl-containing quinoxalin-2(1H)-ones has been developed via the copper-catalyzed cross-coupling reaction of quinoxalin-2(1H)-ones with alcohols with moderate to good yields.

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A facile TBHP-mediated direct oxidative coupling of quinoxalin-2(1H)-ones with arylaldehydes has been developed under metal-free conditions. This method provided a convenient and efficient approach to various 3-acylated quinoxalin-2(1H)-ones from readily available starting materials with excellent regioselectivity. This reaction proceeded efficiently under mild conditions over a broad range of substrates and with functional group tolerance.

An efficient protocol for the synthesis of 3-alkyl quinoxalin-2(1H)-ones has been developed via the transition-metal-free cross-coupling reaction of quinoxalin-2(1H)-ones with ethers with moderate to good yields under relatively mild conditions.