Aug 2026· Nature Communications· Vol 17· 0 citations· 56 references
Medicine
Abstract
Non-thermal plasma (NTP) is a promising approach for activating methane at room temperature, enabling its direct conversion to ethylene under mild conditions. However, the high energy consumption and the trade-off between methane conversion and ethylene selectivity limit its industrial application. Herein, we report a pure-silica self-pillared pentasil (SPP) zeolite catalyst that enables efficient methane conversion to ethylene under non-thermal plasma activation at room temperature. This plasma-catalytic system achieves an exceptional ethylene selectivity of 58.8% with an energy yield of 52 mmol/MJ at atmospheric pressure. Mechanistic studies reveal that isolated hydroxyl groups on the self-pillared pentasil catalyst stabilize gaseous methyl radicals, promoting carbon–carbon coupling and methane dissociation. The confined plasma between catalyst granules selectively suppresses further hydrogenation and methylation of the key C2H5 intermediate, thereby achieving high ethylene selectivity. By systematically adjusting boundary conditions, an ethylene yield of 40% is achieved, surpassing the benchmarks of both plasma and thermal catalytic processes. Non-thermal plasma (NTP) offers a low-temperature route for methane activation but is hindered by high energy consumption and limited ethylene selectivity. Here, the authors develop a pure-silica self-pillared pentasil zeolite that improves methane-to-ethylene conversion under NTP conditions.
Dry reforming of methane (DRM) converts two major greenhouse gases, CH4 and CO2, into syngas. The products (CO and H2) can be directly utilized as feedstock for chemical processes such as Fischer–Tropsch synthesis and methanol production. Transition metal-based catalysts stand as the most commonly employed for DRM on...
Yang Chen, Fei-Yang Hu, Run-Ping Ye et al.· Industrial & Engineering...· 0 citations
Methane valorization is important for climate change mitigation and sustainable carbon utilization, but conventional nonoxidative coupling of methane (NOCM) suffers from the high activation barrier of CH4, limited product selectivity, and rapid coking-induced deactivation. Herein, we develop a spark discharge−dielect...
The reverse water–gas shift (RWGS) reaction is a pivotal step for converting CO2 into value-added chemical intermediates, yet its implementation under industrially relevant high-pressure conditions remains limited by catalyst deactivation, insufficient productivity, and prohibitive material costs. Here, we report a n...
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Low-temperature Fischer-Tropsch synthesis is an energy-efficient process that converts nonpetroleum carbon sources into liquid hydrocarbon fuels. However, achieving C─C coupling under mild conditions is a significant challenge, primary due to the high energy barriers associated with C─O bond cleavage via conventional c...
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Achieving synergistic pollution reduction and carbon mitigation is a key strategy for the iron and steel industry in response to the carbon peaking and carbon neutrality targets. To realize low-energy denitration of sintering flue gas, this work develops a bifunctional catalyst that harvests exothermic heat from CO o...
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Volatile organic compounds (VOCs) are widely considered to inhibit NH3–SCR by competing with NH3 for surface sites and blocking redox centers, yet industrial flue gases frequently contain both VOCs and NOx. Here we show that toluene unexpectedly promotes low-temperature DeNOx over Ce–Ti catalysts, with the hollow nan...
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