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Biochar-layered double hydroxide composites for the adsorption of tetracycline from water: synthesis, process modeling, and mechanism

dc.contributor.authorZubair, Mukarram
dc.contributor.authorDana Essam Alhashim
dc.contributor.authorEl-Qanni, Amjad
dc.contributor.authorMohammad Saood Manzar
dc.contributor.authorAlqahtani, Hissah A.
dc.contributor.authorAl-Ejji, Maryam
dc.contributor.authorMu’azu, Nuhu Dalhat
dc.contributor.authorAlGhamdi, Jwaher M.
dc.contributor.authorHaladu, Shamsuddeen A.
dc.contributor.authorAl-Hashim, Dana
dc.contributor.authorAhmed, Syed Z.
dc.date.accessioned2024-04-03T08:16:35Z
dc.date.available2024-04-03T08:16:35Z
dc.date.issued2023
dc.descriptionQ1
dc.description.abstractAntibiotic-contaminated water is a crucial issue worldwide. Thus, in this study, the MgFeCa-layered double hydroxides were supported in date palm–derived biochar (B) using co-precipitation, hydrothermal, and co-pyrolysis methods. It closes gaps in composite design for pharmaceutical pollutant removal, advances eco-friendly adsorbents, and advances targeted water cleanup by investigating synthesis methodologies and gaining new insights into adsorption. The prepared B-MgFeCa composites were investigated for tetracycline (TC) adsorption from an aqueous solution. The B-MgFeCa composites synthesized through co-precipitation and hydrothermal methods exhibited better crystallinity, functional groups, and well-developed LDH structure within the biochar matrix. However, the co-pyrolysis method resulted in the LDH structure breakage, leading to the low crystalline composite material. The maximum adsorption of TC onto all B-MgFeCa was obtained at an acidic pH range (4–5). The B-MgFeCa composites produced via hydrothermal and co-pyrolysis methods showed higher and faster TC adsorption than the co-precipitation method. The kinetic results can be better described by Langmuir kinetic and mixed order models at low and high TC concentrations, indicating that the rate-limiting step is mainly associated with active binding sites adsorption. The Sip and Freundlich models showed better fitting with the equilibrium data. The TC removal by B-MgFeCa composites prepared via hydrothermal, the highest estimated uptake which is around 639.76 mg.g−1 according to the Sips model at ambient conditions, and co-pyrolysis was mainly dominated by physical and chemical interactions. The composite obtained via the co-precipitation method adsorbed TC through chemical bonding between surface functional groups with anionic species of TC molecule. The B-MgFeCa composite showed excellent reusability performance for up to five cycles with only a 30% decrease in TC removal efficiency. The results demonstrated that B-MgFeCa composites could be used as promising adsorbent materials for effective wastewater treatment.
dc.description.issue50
dc.description.volume30
dc.identifier.doi10.1007/s11356-023-29954-z
dc.identifier.issn1614-7499
dc.identifier.urihttps://doi.org/10.1007/s11356-023-29954-z
dc.identifier.urihttps://repository.iau.edu.sa/handle/123456789/1247
dc.relation.ispartofEnvironmental Science and Pollution Research
dc.subjectEngineered biochar
dc.subjectTetracycline
dc.subjectAdsorption
dc.subjectKinetic and isotherm modeling
dc.titleBiochar-layered double hydroxide composites for the adsorption of tetracycline from water: synthesis, process modeling, and mechanism

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