Publications by authors named "Jinxiao Dou"

Coal-based oxygen electrocatalysts hold immense promise for cost-effective applications in rechargeable Zn-air batteries (ZABs) and the value-added, clean utilization of traditional coal resources. Herein, an electrospun membrane electrode comprising coal-derived carbon nanosheets and directly grown carbon nanotubes (CNS/CMF@CNT) was successfully synthesized. The hierarchical porous structure of the electrode, composed of multiple components, significantly facilitates mass and ion transportation, resulting in exceptional electrochemical performance.

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Among many supercapacitor electrode materials, carbon materials are widely used due to their large specific surface area, good electrical conductivity and high economic efficiency. However, carbon-based supercapacitors face the challenges of low energy density and limited operating environment. This work reports a facile self-assembled method to prepare three-dimensional carbon nanotubes/reduced graphene oxide (CNTs/rGO) aerogel material, which was applied as both positive and negative electrodes in a symmetric superacapacitor.

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Simultaneous capture of SO and NO from flue gas is critical for coal-fired power generation. In this study, environmentally friendly and high-performance deep eutectic solvents based on ethylene glycol and ammonium bromide were designed to capture SO and NO simultaneously. The SO and NO absorption performances and absorption mechanisms were systematically investigated by H NMR and Fourier transform infrared (FT-IR) spectroscopy in combination with ab initio calculations using Gaussian software.

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The removal of NO (approximately 90% of which is NO) from flue gas is a crucial process for clean power generation from coal combustion. Oxidation of NO to NO followed by NO absorption using sorbents is considered to be a promising technology alternative to selective catalytic reduction (SCR). This study investigated the absorption of NO in flue gas by ethylene glycol (EG)-tetrabutylammonium bromide (TBAB) deep eutectic solvents (DESs) under a range of experimental conditions.

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Potassium hydroxide-impregnated char sorbents (KOH/char) prepared via an ultrasonic-assisted method were used for SO removal from flue gas. The desulfurization experiment was analyzed using a fixed-bed reactor under 40-150 °C temperature range, using simulated flue gas. X-ray diffraction (XRD), Fourier-transform infrared spectroscopy, and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDS) were used to analyze both the chemical and physical characteristics of the sorbents.

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Activated carbon has been used commercially to remove SO from coal combustion flue gas. However, the role of inherent CaO in activated carbon is uncertain. In this study, the adverse effects of inherent CaO in the activated carbon derived from coconut shell (CSAC) on its desulfurization performance were systematically studied at the temperature range of 60-100 °C in a fixed-bed reactor.

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The selective absorption of NO in flue gas has been investigated using a series of deep eutectic solvents (DESs) as novel denitrifying agents. The EG-TBAB DESs used in this work are composed of a hydrogen donor ethylene glycol (EG) and a parent salt tetrabutylammonium bromide (TBAB). Effects of DES composition (EG:TBAB molar ratio), operation temperature, residence time, and O concentration in the flue gas on denitrification performances of EG-TBAB DESs have been investigated.

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Oxy-fuel combustion of solid fuels is seen as one of the key technologies for carbon capture to reduce greenhouse gas emissions. The combustion characteristics of lignite coal, Chlorella vulgaris microalgae, and their blends under O2/N2 and O2/CO2 conditions were studied using a Thermogravimetric Analyzer-Mass Spectroscopy (TG-MS). During co-combustion of blends, three distinct peaks were observed and were attributed to C.

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