2022
DOI: 10.3390/cryst12101355
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Fe3O4-Carbon-Based Composite Derived from the Charge-Transfer Reaction Using Waste Tea Leaves as the Carbon Precursor for Enhanced Removing of Azocarmine G2, Methyl Violet 2B, Eosin B, and Toluidine Blue from Aqueous Solution

Abstract: Ferric chloride salt (FeCl3) is a typical vacant orbital acceptor that accepts electrons from urea molecules. This donor-acceptor interaction yields a Fe3O4 oxide, which can be used for preparing novel adsorbent material. Activated carbon (AC) materials, derived from biomass precursors and used for environmental remediation, have gained increasing attention owing to their sustainability, eco-friendly nature, ease of fabrication, and cost-effectiveness. Globally, a large amount of consumed tea leaf materials is… Show more

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Cited by 6 publications
(5 citation statements)
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“…This disordered nature might be due to the presence of abundant functional groups in AO-PC. Generally, the D-to-G-band ratio (I D /I G ) determines the graphitization of the carbon materials [ 37 ]. Here, the I D /I G ratio was calculated as 0.95, reflecting a good graphitization with a partially amorphous portion in the as-prepared AO-PC material, resulting in a moderate degree of graphitization.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…This disordered nature might be due to the presence of abundant functional groups in AO-PC. Generally, the D-to-G-band ratio (I D /I G ) determines the graphitization of the carbon materials [ 37 ]. Here, the I D /I G ratio was calculated as 0.95, reflecting a good graphitization with a partially amorphous portion in the as-prepared AO-PC material, resulting in a moderate degree of graphitization.…”
Section: Resultsmentioning
confidence: 99%
“…This disordered nature might be due to the presence of abundant functional groups in AO-PC. Generally, the D-to-G-band ratio (I D /I G ) determines the graphitization of the carbon materials [37].…”
Section: Structural Characterizations Of As-prepared Ao-pc Materialsmentioning
confidence: 99%
“…Metal-urea complexes were synthesized as follows [9][10][11][12][13]: (i) Six beakers containing 1.0 mmol of each metal chloride salt were dissolved in 25 mL of MeOH solvent (VCl3, ZrOCl28H2O, NbCl5, TaCl5, GaCl3, and TeCl4). Gently heat was used to complete the dissolving of the metal salts.…”
Section: Synthesis Synthesis Of the Metal-urea Complexesmentioning
confidence: 99%
“…The VO2, ZrO2, NbO2, TaO2, Ga2O3, and TeO2 oxides in the nanoscale range were generated by the thermal decomposition of the corresponding primary precursors at 600 °C for 3 hours in ambient air in an electric furnace. After grinding the resulting oxides into a fine powder with particle sizes of approximately ~ 5-6 mm, they were subjected to FT-IR and TEM analyses [9][10][11][12][13].…”
Section: Synthesis Of the Metal Oxidesmentioning
confidence: 99%
“…This carbon material was chemically activated by mixing it with KOH via a 1:3 wt ratio (2 g of carbon material with 6 g of KOH) in a porcelain mortar and crushing the two components into the finest possible powder with a porcelain pestle. The resultant fine mixture was carbonized for 3 h at 600 • C in a tubular furnace in a nitrogen atmosphere which generated the desired activated carbons, which were then cleaned with DI water to remove the potassium compounds and electrical oven dried at 80 • C for 3 h [27][28][29][30][31].…”
Section: Step Twomentioning
confidence: 99%