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Amidst the rapid expansion of the global economy, the demand for energy has escalated. The depletion of traditional energy sources coupled with environmental pollution concerns has catalyzed a shift towards the development and utilization of clean, renewable energy. Biogas, as a renewable energy source, provides diverse applications and holds the potential to alleviate energy shortages. Recently, biogas dry reforming technology has garnered substantial attention as a significant pathway for renewable energy utilization, particularly in the development and optimization of catalysts. Contemporary research predominantly focuses on enhancing the activity and stability of catalysts, with particular emphasis on their resistance to coking and sintering. This review delineates the classification of biogas dry reforming catalysts, their catalytic activity, and issues related to carbon deposition, contrasting biogas dry reforming with traditional dry reforming in catalyst design. It synthesizes numerous studies from recent years aimed at mitigating carbon deposition during the biogas dry reforming process and boosting catalytic activity via active components, carriers, and promoters in both precious and non-precious metal catalysts. Furthermore, it discusses the current challenges of biogas dry reforming technology and outlines prospective future development trends. This discussion provides an in-depth understanding of biogas dry reforming technology and catalyst design, offering insights and recommendations for future research and industrial applications. [ABSTRACT FROM AUTHOR]

Methane is the fundamental raw material of the C1 chemical industry, with abundant reserves. Its direct conversion into high-value-added chemicals has great scientific significance and broad commercial potential for the efficient use of methane resources. However, it is difficult to convert methane into more useful hydrocarbons and hydrogen, as the reaction usually requires external energy to overcome thermodynamic limitations. Non-oxidative coupling of methane to produce ethane and hydrogen is a promising supply technology. Catalysts which can be adapted to various energy sources are key to this technology. In recent years, considerable progress has been made in the design and application of these thermal and photocatalysts. This review outlines some typical catalysts, and reviews the progress in the understanding of reaction mechanisms. Finally, suggestions for the development of high-selectivity and high-stability catalysts for the future are presented. [ABSTRACT FROM AUTHOR]

The present work demonstrates the optimization of the ligand structure in the series of bis(phosphine oxide) and β-ketophosphine oxide representatives for efficient coordination of Tb3+ and Eu3+ ions with the formation of the complexes exhibiting high Tb3+- and Eu3+-centered luminescence. The analysis of the stoichiometry and structure of the lanthanide complexes obtained using the XRD method reveals the great impact of the bridging group nature between two phosphine oxide moieties on the coordination mode of the ligands with Tb3+ and Eu3+ ions. The bridging imido-group facilitates the deprotonation of the imido- bis(phosphine oxide) ligand followed by the formation of tris-complexes. The spectral and PXRD analysis of the separated colloids indicates that the high stability of the tris-complexes provides their safe conversion into polystyrenesulfonate-stabilized colloids using the solvent exchange method. The red Eu3+-centered luminescence of the tris-complex exhibits the same specificity in the solutions and the colloids. The pronounced luminescent response on the antibiotic ceftriaxone allows for sensing the latter in aqueous solutions with an LOD value equal to 0.974 μM. [ABSTRACT FROM AUTHOR]

Methane pyrolysis transforming CH4 into hydrogen without a CO2 byproduct is a potential hydrogen production process under the net-zero emission target. The melt pyrolysis of methane is a technology that could simultaneously obtain hydrogen and carbon products. However, its catalytic activity and stability are still far from satisfactory. In this work, a new strategy for the melt pyrolysis of methane to hydrogen production was proposed using Ni foam and molten NaCl-KCl. The increase in the amount of Ni foam was found to enhance the methane conversion rate from 12.6% to 18%. The process was optimized by the different amounts of catalysts, the height of the Ni foam layer, and the filling method of Ni foam, indicating that the methane conversion rate of the string method could reach 19.2% at 900 °C with the designed aeration device. Furthermore, we observed that the addition of molten salt significantly alleviated the carbon deposition deactivation of the Ni foam and maintained its macrostructure during the reaction. The analysis of the carbon products revealed that carbon black could be obtained. [ABSTRACT FROM AUTHOR]