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Title: | Acetamiprid's degradation products and mechanism: Part II - Inert atmosphere and charge storage | Authors: | Popadić, Daliborka Krstić, Jugoslav Janošević Ležaić, Aleksandra Popović, Maja Milojević-Rakić, Maja Ignjatović, Ljubiša Bajuk-Bogdanović, Danica Gavrilov, Nemanja |
Keywords: | Acetamiprid;Capacitance;Carbonization;Pesticide;Supercapacitor;Thin film | Issue Date: | 16-Dec-2023 | Project: | Ministry of Science, Technological Development and Innovation of the Republic of Serbia (Grants no. 451-03-47/2023-01/200146, 451-03-47/2023-01/200161, 451-03-47/2023-01/ 200017 and 451-03-47/2023-01/200026). | Journal: | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy | Abstract: | Reuse and/or recycling of spent adsorbents is taking a central role in modern thinking and catalyzed carbonization is the way forward. Herein we explore the carbonization of adsorbed acetamiprid, in an inert atmosphere, as a way of recycling and producing nitrogen-rich carbon material for potential use in supercapacitors. Added value material and the reuse of the adsorbent were achieved by carbonization at 700 °C under argon. The formation of a nitrogen-doped carbon layer as an active material on the adsorbent, bonded through a C-Si linkage, has been conclusively verified through elemental composition quantification using XPS and EDX measurements. Two-stage catalytic decomposition and condensation of the adsorbed pesticide is followed by TGA and TPD-MS. Attained carbon-based materials give stable Faradaic capacitance with a slight dependency on the number of adsorbing cycles. Capacitance calculated with respect to the adlayer carbon material reaches values as high as 610 F g-1. Galvanostatic Charge/Discharge measurement confirmed the stability of explored materials with a slight increase in capacitance over 1000 cycles. The presented results envisage electroactive materials preparation from environmental pollutants, adding value to spent adsorbents. |
URI: | https://dspace.ffh.bg.ac.rs/handle/123456789/2170 | DOI: | 10.1016/j.saa.2023.123772 |
Appears in Collections: | Journal Article |
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