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Nonoxidative activation of methane was carried out over Ag/ZSM-5 catalysts, prepared by the wetness impregnation method, and the catalysts were characterized by various techniques. Theoretical calculation was further employed to clarify the reaction mechanism of methane coupling over the catalysts. Ag + ions were found to be the main Ag species at low loading (1-5 wt %) whereas higher loading (10 wt %) resulted in metal clusters. Combined with experimental evidence and computer modeling, it is concluded that isolated Ag + ions play a crucial role in the catalytic coupling of methane under nonoxidative conditions.

An effective way (without addition of any oxidative gases to the reactant) to suppress coke formation (by modification of the Mo/HZSM-5 catalyst) and thus to significantly improve the aromatic selectivity in the methane aromatization reaction is presented in this study. A greater yield of benzene and an enhanced durability of the catalyst when compared with the conventional Mo/HZSM-5 catalysts are observed. Multinuclear solidstate NMR, TPD, TPO, TG, and UV-Raman methods are applied to characterize and rationalize the structureproperty relationship of the improved catalytic performance of the modified catalysts. From this work, we found that only a small fraction of tetrahedral framework aluminum, which corresponds to the Bronsted acid sites, is sufficient to accomplish the aromatization of the intermediates in methane aromatization reaction, while the superfluous strong Bronsted acid sites, which can be removed upon steaming treatment, are shown to be related with the aromatic carbonaceous deposits on the catalysts.

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A novel combined organic and inorganic process for preparing thin supported membrane was developed, using which a thin and defect-free Pd membrane with uniform thickness of 5 microm was directly coated onto porous alpha-Al2O3 hollow fiber without any interlayer and substrate penetration; at the same time, there existed a small interstice between membrane and substrate, which led to higher hydrogen permeance, infinite selectivity, and better membrane stability.

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The accurate and rapid detection of Mycobacterium tuberculosis (M. tuberculosis) is essential for the effective treatment of tuberculosis. In this article, we propose an electrochemical sensor to detect M. tuberculosis reference strain H37Rv. The sensor contains an H37Rv aptamer and oligonucleotides modified with gold nanoparticles (AuNPs− DNA). An H37Rv aptamer screened by our laboratory was used as the recognition probe. The change in frequency shift mediated by AuNPs−DNA in the presence of H37Rv was detected using a multichannel series piezoelectric quartz crystal (MSPQC) system. Three oligonucleotides modified with gold nanoparticles were designed. These oligonucleotides contained 12, 12, and 13 bases that hybridized with the 37-nt H37Rv aptamer. H37Rv aptamer was immobilized on the gold electrode surface by Au−S bonds. A conductive-layer was then formed by sequential hybridization of the aptamer with the three designed AuNPs−DNAs. When H37Rv was present, it specifically bound to the aptamer, resulting in the detachment of AuNPs−DNA from the electrode. The conductive layer was thereby replaced by a nonconductive complex of aptamer and bacteria. These changes were monitored by the MSPQC system. The proposed sensor is rapid, specific and sensitive, the detection time was 2 h. The detection limit was 100 cfu/mL. This sensor would be of great benefit for the early clinical diagnosis of tuberculosis.