5 research outputs found

    A green route for the synthesis of nano-sized hierarchical ZSM-5 zeolite with excellent DTO catalytic performance

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    Nano-sized hierarchical ZSM-5 zeolite with high crystallization was prepared by a novel green strategy, that is, the consecutive freezing and vacuum drying route. In comparison with the traditional synthesis process, only 1/5 amount of TPAOH (tetrapropylammonium hydroxide) template was involved. Moreover, hierarchical structured zeolites can be formed even in the absence of mesoporous template (e. g. cetyltrimethylammonium bromide, CTAB). Moreover, the hierarchical ZSM-5 with a wide range of SiO2/Al2O3 ratio (25–200) can be modulated. The effects of the consecutive freezing and vacuum drying methods on the formation process, pore characteristics, crystallinity, morphology and acidity of the ZSM-5 zeolites were explored. It is noted that the abundant intra-crystal mesopores and nanoparticles structure were generated from the porous structure on the surface of the freeze-dried powder. The constructed nano-sized and hierarchical ZSM-5 catalyst exhibits a prolonged lifetime of 110 h in dimethyl ether-to-olefin (DTO) reaction, which is around 3.7-fold lifetime compared to the conventional microporous ZSM-5

    Engineering Ni/SiOâ‚‚ catalysts for enhanced COâ‚‚ methanation

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    The CO₂ methanation is an important process in coal-to-gas, power-to-gas and CO₂ removal for spacecraft. Recently, metal-organic framework (MOF) derivatives have been demonstrated as high-performance catalysts for CO₂ upgrading processes. However, due to the high costs and low stability of MOF derivatives, it still remains challenge for the development of alternative synthesis methods avoiding MOF precursors. In this work, we present the sol-gel method for loading Ni-MOF to silica support in two-steps. Upon modifying the procedure, a more simplified one-step sol-gel method has been developed. Furthermore, the obtained Ni/SiO₂ catalyst still exhibits great catalytic performance with a CO₂ conversion of 77.2% and considerable CH4 selectivity of ~100% during a stability test for 52 h under a low temperature of 310 °C and high GHSV of 20,000 mL·g−1·h−1. Therefore, this work provides a ground-breaking direct strategy for loading MOF derived catalysts, and might shed a light on the preparation of highly dispersed Ni/SiO₂ catalyst

    Catalyst-free synthesis of amines from cyclic ketones and formamides in superheated water

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    <p>A novel and environmentally benign protocol for the synthesis of amines from cyclic ketones and formamides is demonstrated. The reaction proceeds under catalyst-free and superheated water conditions and yields range from poor to excellent.</p

    Regio- and stereoselective co-iodination of olefins using NH<sub>4</sub>I and Oxone

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    <p>A simple, efficient, and environmentally benign protocol for the synthesis of vicinal iodohydrins and iodoesters from olefins using NH<sub>4</sub>I and Oxone in CH<sub>3</sub>CN/H<sub>2</sub>O (1:1) and dimethylformamide (DMF) / dimethylacetamide (DMA), respectively, without employing a catalyst at room temperature is described. Regio- and stereoselective iodohydroxylation and iodoesterification of various olefins with <i>anti</i> fashion, following Markonikov’s rule, was achieved and the corresponding products were obtained in good to excellent yields. In addition, 1,2-disubstituted olefins afforded excellent diastereoselectivity.</p
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