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Microwave method speeds coal based carbon for CO2 capture
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Microwave method speeds coal based carbon for CO2 capture

by Riko Seibo
Tokyo, Japan (SPX) Feb 16, 2026

Scientists have demonstrated a rapid microwave based method to produce advanced coal derived carbon materials capable of capturing carbon dioxide, a major greenhouse gas driving climate change. The new process significantly shortens preparation time while maintaining or improving adsorption performance compared to conventional heating methods.

The research team developed a strategy that combines a pre oxidation step with microwave activation to create nitrogen doped ultramicroporous carbon from Ningdong coal. This approach uses volumetric microwave heating to quickly activate the carbon precursor while preserving nitrogen and oxygen functional groups that enhance CO2 adsorption.

Traditional routes to carbon based adsorbents often rely on long periods of high temperature furnace heating, sometimes exceeding an hour, which consumes large amounts of energy and can degrade key surface functionalities. In contrast, the microwave synthesis method can generate high quality activated carbon in about ten minutes while keeping microwave absorption efficiency high, leading to much lower overall energy consumption.

Before microwave activation, the coal undergoes an oxidative pretreatment that introduces oxygen containing active sites. These sites promote the efficient incorporation of nitrogen atoms during subsequent microwave processing, resulting in a carbon material with a high density of adsorption active sites and a rich population of ultramicropores tailored for gas capture.

The resulting ultramicroporous carbon features pore widths between 0.6 and 0.7 nanometers, dimensions that closely match the kinetic diameter of CO2 molecules. This fine pore structure supports strong molecular confinement effects, boosting the physical adsorption of carbon dioxide relative to larger gas molecules.

Experimental measurements showed that the optimized sample reached a CO2 uptake of 4.72 millimoles per gram at zero degrees Celsius and 3.33 millimoles per gram at room temperature. The material also exhibited strong selectivity for CO2 over nitrogen, an essential characteristic for gas separation processes such as flue gas treatment.

Beyond adsorption capacity and selectivity, the work highlights the energy savings enabled by microwave processing. Conventional activation in high power furnaces over extended times typically demands large electricity inputs, while the rapid microwave route cuts processing time and lowers energy consumption by nearly two orders of magnitude.

The study further clarifies how surface chemistry and pore structure work together to determine carbon capture performance. Increasing nitrogen doping strengthens the chemical affinity of the carbon surface for CO2, while the ultramicroporous network enhances physical adsorption, and the combination yields high overall uptake and selectivity.

According to the researchers, "Carbon capture technologies must become faster, more efficient, and scalable if we hope to meet global climate targets." They note that microwave assisted synthesis offers a way to improve material performance while at the same time reducing the energy requirements of production.

The scalable nature of the method is another important outcome. Because the process uses inexpensive coal as a starting material and relies on rapid microwave heating rather than long furnace cycles, it offers strong potential for industrial scale manufacturing of advanced adsorbents for carbon capture and gas separation.

As demand grows for technologies that can help reduce greenhouse gas emissions, the team argues that innovations like this microwave based synthesis route will be increasingly important. The work provides a framework for designing next generation porous carbon materials that combine tailored surface functionality with carefully engineered ultramicropore structures.

Research Report: Rapid microwave synthesis of nitrogen-doped ultramicroporous coal-based carbon with enhanced CO2 adsorption performance

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