2022
DOI: 10.1016/j.micromeso.2022.111848
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N-doped activated carbon for high-efficiency ofloxacin adsorption

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Cited by 46 publications
(19 citation statements)
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“…In the near-neutral range, groups such as –OH and –NH 2 in the OFX molecular structure could form hydrogen bonds with the oxygen-containing functional groups protonated on the FMBC surface to promote adsorption. 53 In addition, the OFX molecules that contained zwitterions had the lowest solubility and the highest hydrophobicity and that promoted the OFX molecules to fast reach FMBC surfaces, 54 which resulted in the highest OFX adsorption at pH 7 under hydrogen bonding and hydrophobic interactions. As the pH continued to increase from 7 to 12, the adsorption capacity of FMBC was significantly decreased due to the greater electrostatic repulsion between the negatively charged surface of FMBC and OFX − and the large amount of OH − in the solution prevented OFX from entering the FMBC surface.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In the near-neutral range, groups such as –OH and –NH 2 in the OFX molecular structure could form hydrogen bonds with the oxygen-containing functional groups protonated on the FMBC surface to promote adsorption. 53 In addition, the OFX molecules that contained zwitterions had the lowest solubility and the highest hydrophobicity and that promoted the OFX molecules to fast reach FMBC surfaces, 54 which resulted in the highest OFX adsorption at pH 7 under hydrogen bonding and hydrophobic interactions. As the pH continued to increase from 7 to 12, the adsorption capacity of FMBC was significantly decreased due to the greater electrostatic repulsion between the negatively charged surface of FMBC and OFX − and the large amount of OH − in the solution prevented OFX from entering the FMBC surface.…”
Section: Resultsmentioning
confidence: 99%
“…6(a), in terms of coexisting anions, the addition of SO 4 2− had a small enhancement on the adsorption, which may be due to ionic hydrolysis reactions and the formation of a small amount of hydrogen bonds. 53,56 The addition of Cl − had little effect on the adsorption capacity, and when the Cl − concentration was 0.01 mol L −1 , it promoted the adsorption process, probably because the solubility of OFX was reduced by salting out, and therefore the adsorption capacity was enhanced. 56 However, the addition of NO 3 − , CO 3 2− , and PO 4 3− showed a significant decrease in the adsorption capacity.…”
Section: Resultsmentioning
confidence: 99%
“…The BET isotherm was calculated by Eqs. 1 and 2 leading to the general adsorption isotherm GAI 25, 26. truenormalGAI=N( p p0 )= normalWnormalmin normalWnormalmax N( p p0 ,W)f(W)normaldW truenormalGAI= 1 [W( p p0 )-1] …”
Section: Methodsmentioning
confidence: 99%
“…The BET isotherm was calculated by Eqs. ( 1) and ( 2) leading to the general adsorption isotherm GAI [25,26].…”
Section: Porosity and Adsorption Measurements Based On Brunauer-emmet...mentioning
confidence: 99%
“…Therefore, the analysis of experimental data with these models provides important information for the design of the adsorption process as an operation unit and attributes further comprehension into the mechanism of the adsorption process and economic considerations [25][26][27] . In general, experimental data obtained in the adsorption of phenol by various adsorbents have been discussed using Freundlich, Langmuir, Dubinin-Radushkevich, Temkin, and Liu models 28,29 . However, the interpretation of phenol adsorption properties using these models is limited due to the disability of these models to understand the complete adsorption process and the parameters affecting the process.…”
Section: Toward a Mechanistic Understanding Of Adsorption Behavior Of...mentioning
confidence: 99%