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Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole.

ABSTRACT: Using organic salts as precursors, heteroatom-doped porous carbons prepared by in situ activation had surface areas of up to 2703 m² g^-1. These porous carbons have been found to be effective adsorbents for adsorption of sulfamethoxazole (SMX) from water. The effects of precursor type, calcination temperature, pH and ionic strength as well as the regeneration properties were investigated. The different adsorption performances of porous carbons were related to their textural structures and chemical properties, and a reasonable adsorption mechanism was proposed. The effects of different heteroatom functional groups on the adsorption of SMX were also analyzed in detail. For potential practical applications, the performance of the porous carbon for removing SMX from real water was also tested.

SUBMITTER: Zheng W

PROVIDER: S-EPMC9047560 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole.

Zheng Wei W Shi Yawei Y Liu Guozhu G Zhao Bin B Wang Liang L

RSC advances 20200108 3

Using organic salts as precursors, heteroatom-doped porous carbons prepared by in situ activation had surface areas of up to 2703 m2 g-1. These porous carbons have been found to be effective adsorbents for adsorption of sulfamethoxazole (SMX) from water. The effects of precursor type, calcination temperature, pH and ionic strength as well as the regeneration properties were investigated. The different adsorption performances of porous carbons were related to their te ...[more]

PMID: 35494670

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Project description:Two novel carbons (MCs) derived from moxa floss of different storage years have been prepared by two low-cost and facile approaches, which are hydrothermal carbonization at a low temperature (200 °C) and direct pyrolysis at a moderate temperature (500 °C) followed by potassium hydroxide (KOH) activation strategy at a high temperature (800 °C), respectively. The physicochemical properties of MCs are investigated by Raman spectra, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and nitrogen adsorption-desorption isotherms. Results show that MCs derived from moxa floss of different storage years by two facile approaches possess different morphologies: MCs by hydrothermal carbonization (denoted as MC-1, MC-2 and MC-3) exhibit porous nanosheet structures, the highest specific surface area is about 1788.6 m2 g-1, and the largest total pore volumes is around 0.8170 cm3 g-1, while MCs by direct pyrolysis (denoted as MC-4, MC-5 and MC-6) have basically blocky and rod-like morphologies, the highest specific surface area is about 1628.0 m2 g-1, and the largest total pore volume is around 0.7058 cm3 g-1. However, despite the different morphologies, all MCs possess a similar hierarchical porous structure, numerous heteroatom groups and good electrical conductivity. Therefore, these low-cost, biomass-derived porous carbons with promising capacitive performance are used for supercapacitors application with high performance, for example, the as-assembled supercapacitor based on MC-5 exhibits a high specific capacitance of 288.3 F g-1 at 0.25 A g-1, an excellent rate performance of 243.5 F g-1 even at 30 A g-1 with 84.5% capacitance retention of its initial specific capacitance, and an outstanding long-term cycling stability with 98.7% capacitance retention after 10 000 cycles at 5 A g-1. Furthermore, the maximum energy density for these supercapacitors with an aqueous electrolyte in a two-electrode system is about 10.0 W h kg-1 at a power density of 70.3 W kg-1. Therefore, this work opens up a whole new field for the applications of moxa floss and this novel concept of moxa floss use is an extremely promising strategy for developing high-performance carbons with porous structures and heteroatom-doping from renewable sources.

Dataset Information

Heteroatom-doped highly porous carbons prepared by in situ activation for efficient adsorptive removal of sulfamethoxazole.

Publications

Heteroatom-doped highly porous carbons prepared by <i>in situ</i> activation for efficient adsorptive removal of sulfamethoxazole.

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