Effective factors on performance of zeolite based metal catalysts in light hydrocarbon aromatization

Aromatic hydrocarbons are essential compounds, that the presence of which in fuels can improve the octane number. The conversion of the light alkanes to high value aromatics is vital from theoretical and industrial standpoints. Zeolites such as ZSM-5 play an essential role in the aromatization of light alkanes. This paper highlights the mechanism of aromatization of light alkanes such as methane, ethane, propane, butane, and its isomers. Furthermore, effective factors on the aromatization of light alkanes including metal type, crystallinity, acidity, space velocity, pretreatment of zeolites, co-feeding of light hydrocarbon, and operating factors such as temperature have been investigated to determine how a system of zeolite with metals can be useful to reach aromatization with high conversion.

Light alkane oxidation over well-defined active sites in metal–organic framework materials

We review structure–catalytic property relationships for MOF materials used in the direct oxidation of light alkanes, focusing specifically on the elucidation of active site structures and probes for reaction mechanisms.

Recent progress in Cr-based catalysts for oxidative dehydrogenation of light alkanes by employing CO2 as a soft oxidant

CO2 can be used as a soft oxidant for oxidative dehydrogenation of light alkanes (CO2-ODH), which is beneficial to realize the reuse of CO2 and meet the demand for olefins. The core of this reaction is the catalyst. Cr-based catalysts have attracted much attention for their excellent catalytic performance in CO2-ODH reactions due to their various oxidation states and local electronic structures. In this paper, the synthesis and modification methods of Cr-based catalysts for CO2-ODH are reviewed. The structure–activity relationship and reaction mechanism are also summarized. Moreover, the reasons for the deactivation of Cr-based catalysts are analysed and the main challenges faced by Cr-based catalysts in the CO2-ODH process, as well as the future development trend and prospect, are discussed.

Th-MOF showing six-fold imide-sealed pockets for middle-size-separation of propane from nature gas

Separation of propane from nature gas is of great importance to industry. However, in light of size-based separation, there still lacks effective method to directly separate propane from nature gas, due to the comparable physical properties for these light alkanes (C1-C4) and the middle size of propane. In this work, we found that a new Th-MOF could be an ideal solution for this issue. The Th-MOF takes UiO-66-type structure, but with the pocket sealed by six-fold imide groups; this not only precisely reduces the size of pocket to exactly match propane, but also enhances the host-guest interactions through multiple supramolecular interactions. As a result, highly selective adsorption of propane over methane, ethane, and butane was observed, implying unique middle-size separation. The actual separation was confirmed by breakthrough experiments, and it is found that both relatively smaller molecules (methane and ethane) and relatively bigger molecules (butane) break through the Th-MOF column within 10 min/g, whereas propane with middle size can maintain very long retention time up to 80 min/g, strongly suggesting middle-size separation and its superior application in direct separation of propane from nature gas. The separation mechanism, as unveiled by both theoretical calculation and comparative experiments, is due to the six-fold imide-sealed pockets that could effectively distinguish propane from other light alkanes through both size effect and host-guest interactions.