Waste to resource approach: CoFe2O4-modified spent tea waste for magnetic solid-phase extraction of toxic metal ions from water samples

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In this research, within the framework of a waste-to-resource conversion approach, biochar obtained from spent tea waste (STWB), a widely available and cost-free biomass source, was modified with magnetic CoFe2O4 nanoparticles to develop an environmentally friendly adsorbent (CoFe2O4/STWB). The applicability of this material for efficient separation and preconcentration of Cd(ii), Pb(ii), and Ni(ii) ions from mining wastewater, stream water, and wastewater samples collected from an organized industrial zone was systematically investigated using the solid phase extraction (SPE) method. Optimization of the experimental variables was conducted to enhance the extraction performance of the target analyte ions. The fact that the adsorption and desorption equilibrium times occur in less than 1 min demonstrates the rapid and highly efficient extraction performance of the developed adsorbent. Langmuir isotherm model analysis revealed that CoFe2O4/STWB exhibits adsorption capacities of 69.4 mg g−1 for Cd(ii), 185.2 mg g−1 for Pb(ii), and 45.2 mg g−1 for Ni(ii). In contrast, the corresponding adsorption capacities obtained for unmodified STWB were considerably lower, with values of 42.9, 75.8, and 16.8 mg g−1 for Cd(ii), Pb(ii), and Ni(ii), respectively. These results clearly demonstrate that modification with CoFe2O4 significantly enhances the adsorption performance of STWB. Consequently, CoFe2O4-modified spent tea waste can be regarded as an effective, economical, and sustainable adsorbent for trace heavy metal analysis in environmental water samples, owing to its rapid extraction kinetics, high adsorption capacity, and low detection limits. This journal is

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/12320Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1039/d6ay00152aYayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorSeker, Serdal
dc.contributor.authorOzdes, Duygu
dc.contributor.authorDuran, Celal
dc.date.accessioned2026-10-22T10:19:57.030040466Z
dc.date.available2026-10-22T10:19:57.030040466Z
dc.date.issued2026
dc.description.abstractIn this research, within the framework of a waste-to-resource conversion approach, biochar obtained from spent tea waste (STWB), a widely available and cost-free biomass source, was modified with magnetic CoFe2O4 nanoparticles to develop an environmentally friendly adsorbent (CoFe2O4/STWB). The applicability of this material for efficient separation and preconcentration of Cd(ii), Pb(ii), and Ni(ii) ions from mining wastewater, stream water, and wastewater samples collected from an organized industrial zone was systematically investigated using the solid phase extraction (SPE) method. Optimization of the experimental variables was conducted to enhance the extraction performance of the target analyte ions. The fact that the adsorption and desorption equilibrium times occur in less than 1 min demonstrates the rapid and highly efficient extraction performance of the developed adsorbent. Langmuir isotherm model analysis revealed that CoFe2O4/STWB exhibits adsorption capacities of 69.4 mg g−1 for Cd(ii), 185.2 mg g−1 for Pb(ii), and 45.2 mg g−1 for Ni(ii). In contrast, the corresponding adsorption capacities obtained for unmodified STWB were considerably lower, with values of 42.9, 75.8, and 16.8 mg g−1 for Cd(ii), Pb(ii), and Ni(ii), respectively. These results clearly demonstrate that modification with CoFe2O4 significantly enhances the adsorption performance of STWB. Consequently, CoFe2O4-modified spent tea waste can be regarded as an effective, economical, and sustainable adsorbent for trace heavy metal analysis in environmental water samples, owing to its rapid extraction kinetics, high adsorption capacity, and low detection limits. This journal is
dc.description.sponsorshipGümüşhane Üniversitesi, GU, (E0116.07.01)
dc.identifier.doi10.1039/d6ay00152a
dc.identifier.eissn1759-9679
dc.identifier.endpage2811
dc.identifier.issn1759-9660
dc.identifier.issue13
dc.identifier.pmid41878950
dc.identifier.scopus2-s2.0-105033808128
dc.identifier.startpage2799
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/12320
dc.identifier.volume18
dc.identifier.wosWOS:001722398100001
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofAnalytical Methods
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject.classificationChemistry, Analytical
dc.subject.classificationFood Science & Technology
dc.subject.classificationSpectroscopy
dc.subject.classificationChemistry
dc.subject.otherAdsorption
dc.subject.otherCobalt compounds
dc.subject.otherIron compounds
dc.subject.otherIsotherms
dc.subject.otherLead compounds
dc.subject.otherMetal analysis
dc.subject.otherMetal ions
dc.subject.otherNanomagnetics
dc.subject.otherPhase separation
dc.subject.otherTea
dc.subject.otheradsorbent
dc.subject.otherheavy metal
dc.subject.otherlead
dc.subject.othermetal ion
dc.subject.otherAdsorption capacities
dc.subject.otherBiochar
dc.subject.otherBiomass source
dc.subject.otherMagnetic solid-phase extractions
dc.subject.otherPerformance
dc.subject.otherPre-concentration
dc.subject.otherResource conversion
dc.subject.otherTea wastes
dc.subject.otherToxic metal ions
dc.subject.otherWater samples
dc.subject.otherarticle
dc.subject.otherbiomass
dc.subject.othercharcoal
dc.subject.othercontrolled study
dc.subject.otherdesorption
dc.subject.otherisotherm
dc.subject.otherlimit of detection
dc.subject.othersolid phase extraction
dc.subject.otherwaste
dc.subject.otherwater
dc.subject.otherExtraction
dc.titleWaste to resource approach: CoFe2O4-modified spent tea waste for magnetic solid-phase extraction of toxic metal ions from water samples
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus1
rdl.citation.wos1
rdl.departmentGumushane University, Graduate School of Education, Gumushane, 29100, Türkiye
rdl.departmentGumushane University, Gumushane Vocational School, 29100, Gumushane, Türkiye
rdl.oa.statushybrid
rdl.oa.urlhttps://pubs.rsc.org/en/content/articlepdf/2026/ay/d6ay00152a
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)