C₂₊ hydrocarbons, especially C₂₊ olefins, as important basic chemical raw materials, mainly come from petroleum cracking. With the increasing scarcity of petroleum resources, the search for new olefins production routes has become the focus of research, and the production of olefins by the oxidative coupling of methane (OCM) process has attracted extensive attention. The OCM route is an important alternative to the production of olefins from petroleum resources and is also an important direction for the development of efficient and clean utilization of natural gas. In this paper, the mechanism, catalysts, and other key factors for the production of olefins by methane oxidative coupling are reviewed. The mechanism of OCM, including the reaction pathway and the formation of intermediate products, is introduced. Then, commonly used catalysts, such as alkali metal/alkaline earth metal oxides, rare earth metal oxides, composite metal oxides with special structures, and classical catalysts Mn/Na₂WO₄/SiO₂, and their mechanisms of action in the reaction are discussed. In addition, the application of chemical looping oxidative coupling of methane (CLOCM) in olefin production is also investigated, which is a promising alternative way due to the high selectivity of olefins and the low cost of catalysts owing to the excellent performance of the catalyst recycling. These studies will help to further understand the mechanism of OCM for olefin production and provide guidance and support for applications in related fields.

To reveal the effect of torrefaction pretreatment on pyrolysis and gasification reactivity of biomass, corn cob was first subjected to torrefaction pretreatment in a fixed-bed reactor at various reaction temperatures. The pyrolysis reactivity, kinetics, and gasification reactivity of torrefied corn cob were systematically assessed by various methods, proving that torrefaction pretreatment has a substantial influence on the physicochemical properties of corn cobs. The O/C and H/C molar ratios of corn cobs considerably drop with the increasing torrefaction temperature, and their higher heat-ing value (HHV) and energy density rise as well. It is found that torrefaction improves the pyrolysis reactivity of corn cobs because hemicellulose degradation is more severe than cellulose degradation during torrefaction, resulting in an increase in the percentage of cellulose in torrefied corn cobs. However, the severe depolymerization, polycondensation, and carbonization reaction during torre-faction of corn cobs at 280–300 °C can lead to a significant decline in the pyrolysis reactivity of corn cobs. Torrefaction pretreatment increases the pyrolysis activation energy of corn cobs, in addition to decreasing the char gasification reactivity of corn cob. The average char gasification reactivity of corn cobs drops when torrefaction severity increases. The passivation of active sites on the char surface may cause condensation and carbonation reactions of corn cobs during torrefaction. These findings provide new sights into the reasonable design of efficient torrefaction methods for appli-cation prior to pyrolysis and gasification of biomass.

The catalytic fast pyrolysis (CFP) of bio-derived furans offers a promising approach for sustainable aromatic production. ZSM-5 modified by different metal species (Zn, Mo, Fe, and Ga) was employed in the CFP of bio-derived furans for enhancing aromatic production. The effects of metal species, metal loadings, and the weight hourly space velocity (WHSV) on the product distributions from the CFP of 2-methylfuran (MF) were systemically investigated. It is found that the introduction of Zn, Mo, Fe, and Ga on ZSM-5 significantly increases the MF conversion and aromatic yields. The maximum MF conversions of 75.49 and 69.03% are obtained, respectively, by Fe-ZSM-5 and Ga-ZSM-5, which boost the aromatic yield by 34.5 and 42.7% compared to ZSM-5. The optimal loading of Fe on ZSM-5 is 2%. Additionally, the highest aromatic yield of 40.03% is achieved by 2%Fe-ZSM-5 at a WHSV of 2 h⁻¹. The catalyst characterization demonstrates that the synergistic effect of Brønsted and Lewis acid sites in Fe-ZSM-5 is responsible for achieving the efficient aromatization of MF. The key to designing improved zeolite catalysts for MF aromatization is the introduction of large numbers of new Lewis acid sites without a significant loss of Brønsted acid sites in ZSM-5. These findings can provide guidelines for the rational design of better zeolite catalysts used in the CFP of biomass and its derived furans.

A lightweight and high-efficiency microwave-absorbing material was developed via an in situ solvothermal pyrolysis strategy by anchoring sphere-like Fe₃O₄ nanostructures onto bamboo-derived porous carbon (BPC). The resulting composites preserve the intrinsic anisotropic honeycomb architecture of bamboo while introducing uniformly distributed magnetic nanoparticles, enabling synergistic dielectric–magnetic loss. Electromagnetic parameters, alongside impedance matching, were successfully modulated through the optimization of precursor concentrations. Of the evaluated materials, BPC-0.9 stood out for its intense attenuation, recording an RL_min of −45.17 dB at a 1.8 mm thickness. Furthermore, a significant effective absorption bandwidth of 6.65 GHz was attained by the BPC-0.6 sample at only 2.2 mm. Several factors contribute to the boosted efficiency, starting with conductive and interfacial polarization losses paired with multiple scattering events. Furthermore, magnetic loss components, encompassing eddy current effects as well as natural and exchange resonances, play a pivotal role in optimizing the material’s response. Furthermore, radar cross-section (RCS) modeling reveals a substantial reduction of 19.9 dB·m², verifying the material’s viability for real-world stealth technologies. Our findings offer a straightforward methodology for fabricating magnetic carbon structures from biomass with adjustable dielectric responses, underscoring their potential in high-performance energy conversion and low-density microwave absorption.