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Article: The Adsorption Behaviors and Mechanisms of Humic Substances by Thermally Oxidized Graphitic Carbon Nitride

TitleThe Adsorption Behaviors and Mechanisms of Humic Substances by Thermally Oxidized Graphitic Carbon Nitride
Authors
Keywordsadsorption removal
electrostatic interactions
humic substances
π-π interactions
Issue Date2023
Citation
Toxics, 2023, v. 11, n. 4, article no. 369 How to Cite?
AbstractThermal oxidation is efficient for enhancing the photocatalysis performance of graphitic carbon nitride (g-C3N4), while its effect on adsorption performance has not been fully studied, which is crucial to the application of g-C3N4 as adsorbents and photocatalysts. In this study, thermal oxidation was used to prepare sheet-like g-C3N4 (TCN), and its application for adsorption of humic acids (HA) and fulvic acids (FA) was evaluated. The results showed that thermal oxidation clearly affected the properties of TCN. After thermal oxidation, the adsorption performance of TCN was enhanced significantly, and the adsorption amount of HA increased from 63.23 (the bulk g-C3N4) to 145.35 mg/g [TCN prepared at 600 °C (TCN-600)]. Based on fitting results using the Sips model, the maximum adsorption amounts of TCN-600 for HA and FA were 327.88 and 213.58 mg/g, respectively. The adsorption for HA and FA was markedly affected by pH, alkaline, and alkaline earth metals due to electrostatic interactions. The major adsorption mechanisms included electrostatic interactions, π-π interactions, hydrogen bonding, along with a special pH-dependent conformation (for HA). These findings implied that TCN prepared from environmental-friendly thermal oxidation showed promising prospects for humic substances (HSs) adsorption in natural water and wastewater.
Persistent Identifierhttp://hdl.handle.net/10722/344526

 

DC FieldValueLanguage
dc.contributor.authorLi, Hongxin-
dc.contributor.authorWang, Jianlong-
dc.contributor.authorYue, Dongbei-
dc.contributor.authorWang, Jianchao-
dc.contributor.authorTang, Chu-
dc.contributor.authorZhang, Lingyue-
dc.date.accessioned2024-07-31T03:04:14Z-
dc.date.available2024-07-31T03:04:14Z-
dc.date.issued2023-
dc.identifier.citationToxics, 2023, v. 11, n. 4, article no. 369-
dc.identifier.urihttp://hdl.handle.net/10722/344526-
dc.description.abstractThermal oxidation is efficient for enhancing the photocatalysis performance of graphitic carbon nitride (g-C3N4), while its effect on adsorption performance has not been fully studied, which is crucial to the application of g-C3N4 as adsorbents and photocatalysts. In this study, thermal oxidation was used to prepare sheet-like g-C3N4 (TCN), and its application for adsorption of humic acids (HA) and fulvic acids (FA) was evaluated. The results showed that thermal oxidation clearly affected the properties of TCN. After thermal oxidation, the adsorption performance of TCN was enhanced significantly, and the adsorption amount of HA increased from 63.23 (the bulk g-C3N4) to 145.35 mg/g [TCN prepared at 600 °C (TCN-600)]. Based on fitting results using the Sips model, the maximum adsorption amounts of TCN-600 for HA and FA were 327.88 and 213.58 mg/g, respectively. The adsorption for HA and FA was markedly affected by pH, alkaline, and alkaline earth metals due to electrostatic interactions. The major adsorption mechanisms included electrostatic interactions, π-π interactions, hydrogen bonding, along with a special pH-dependent conformation (for HA). These findings implied that TCN prepared from environmental-friendly thermal oxidation showed promising prospects for humic substances (HSs) adsorption in natural water and wastewater.-
dc.languageeng-
dc.relation.ispartofToxics-
dc.subjectadsorption removal-
dc.subjectelectrostatic interactions-
dc.subjecthumic substances-
dc.subjectπ-π interactions-
dc.titleThe Adsorption Behaviors and Mechanisms of Humic Substances by Thermally Oxidized Graphitic Carbon Nitride-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.3390/toxics11040369-
dc.identifier.scopuseid_2-s2.0-85153747762-
dc.identifier.volume11-
dc.identifier.issue4-
dc.identifier.spagearticle no. 369-
dc.identifier.epagearticle no. 369-
dc.identifier.eissn2305-6304-

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