Valorization of tea industry waste into boric acid–activated carbon for phenol removal from aqueous solutions

MakaleYalnız künye
  • SDG 6 · Temiz Su ve Sanitasyon
  • SDG 12 · Sorumlu Üretim ve Tüketim

Özet

The tea industry generates substantial quantities of solid waste with limited high-value industrial applications. In this study, tea industry waste was converted into boric acid-activated carbon (BA–TAC) through a simple one-step chemical activation process and evaluated as an adsorbent for phenol removal from aqueous solutions. BA–TAC exhibited a mixed micro–mesoporous structure with a BET surface area of 592.59 m2 g−1. The adsorption performance was investigated as a function of solution pH, contact time, and initial phenol concentration. Adsorption kinetics were evaluated using pseudo-first order, pseudo-second order, Elovich, Avrami, and intraparticle diffusion models, whereas equilibrium data were analyzed using Langmuir, Freundlich, and Sips isotherms. Linear, pseudo-linear, and non-linear regression approaches were comparatively evaluated, demonstrating the limitations of conventional linearization and the superiority of direct non-linear regression. Moreover, the so-called linearized forms of multi-parameter models such as Sips are not truly linear because iterative parameter estimation remains necessary. The maximum experimental phenol adsorption capacity reached 101.80 mg g−1 despite the moderate BET surface area of BA–TAC. The experimentally determined natural pH and pHpzc values, together with the limited desorption efficiency, indicated that adsorption was governed predominantly by surface chemical interactions rather than electrostatic attraction alone. XPS analysis confirmed the incorporation of boron-containing surface functionalities, highlighting their contribution to phenol adsorption. Overall, this study demonstrates the successful valorization of tea industry waste into a functional boron-modified activated carbon while providing methodological guidance for reliable adsorption kinetics and equilibrium modeling, thereby supporting sustainable waste valorization.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/gumushane/12246Resmi atıflarda kullanılan kalıcı adres
Tam Kayıt
AlanDeğerDil
dc.contributor.authorDuran, Celal
dc.contributor.authorOzdes, Duygu
dc.contributor.authorOzdemir, Olcay
dc.contributor.authorOnal, Yunus
dc.contributor.authorGundogdu, Ali
dc.date.accessioned2026-10-22T10:19:51.591523534Z
dc.date.available2026-10-22T10:19:51.591523534Z
dc.date.issued2026
dc.description.abstractThe tea industry generates substantial quantities of solid waste with limited high-value industrial applications. In this study, tea industry waste was converted into boric acid-activated carbon (BA–TAC) through a simple one-step chemical activation process and evaluated as an adsorbent for phenol removal from aqueous solutions. BA–TAC exhibited a mixed micro–mesoporous structure with a BET surface area of 592.59 m2 g−1. The adsorption performance was investigated as a function of solution pH, contact time, and initial phenol concentration. Adsorption kinetics were evaluated using pseudo-first order, pseudo-second order, Elovich, Avrami, and intraparticle diffusion models, whereas equilibrium data were analyzed using Langmuir, Freundlich, and Sips isotherms. Linear, pseudo-linear, and non-linear regression approaches were comparatively evaluated, demonstrating the limitations of conventional linearization and the superiority of direct non-linear regression. Moreover, the so-called linearized forms of multi-parameter models such as Sips are not truly linear because iterative parameter estimation remains necessary. The maximum experimental phenol adsorption capacity reached 101.80 mg g−1 despite the moderate BET surface area of BA–TAC. The experimentally determined natural pH and pHpzc values, together with the limited desorption efficiency, indicated that adsorption was governed predominantly by surface chemical interactions rather than electrostatic attraction alone. XPS analysis confirmed the incorporation of boron-containing surface functionalities, highlighting their contribution to phenol adsorption. Overall, this study demonstrates the successful valorization of tea industry waste into a functional boron-modified activated carbon while providing methodological guidance for reliable adsorption kinetics and equilibrium modeling, thereby supporting sustainable waste valorization.
dc.description.sponsorshipScientific Research Projects Coordination Unit of Karadeniz Technical University, (FBA-2022-10498)
dc.identifier.articlenumber115784
dc.identifier.doi10.1016/j.wasman.2026.115784
dc.identifier.eissn1879-2456
dc.identifier.issn0956-053X
dc.identifier.pmid42556080
dc.identifier.scopus2-s2.0-105046537150
dc.identifier.startpage115784
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/gumushane/12246
dc.identifier.volume225
dc.identifier.wosWOS:001844386400001
dc.language.isoen
dc.publisherElsevier Ltd
dc.relation.ispartofWaste Management
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBoric acid–activated carbon
dc.subjectKinetic and isotherm analysis
dc.subjectLinear, pseudo-linear and non-linear adsorption modeling
dc.subjectPhenol removal
dc.subjectTea industry waste
dc.subjectWaste valorization
dc.subject.classificationEngineering, Environmental
dc.subject.classificationEnvironmental Sciences
dc.subject.classificationEngineering
dc.subject.classificationEnvironmental Sciences & Ecology
dc.subject.otherAdsorption
dc.subject.otherBoric Acids
dc.subject.otherCharcoal
dc.subject.otherHydrogen-Ion Concentration
dc.subject.otherIndustrial Waste
dc.subject.otherKinetics
dc.subject.otherPhenol
dc.subject.otherTea
dc.subject.otherWaste Disposal, Fluid
dc.subject.otherWater Pollutants, Chemical
dc.subject.otherActivated carbon
dc.subject.otherAdsorption isotherms
dc.subject.otherBoride coatings
dc.subject.otherBoron
dc.subject.otherChemical activation
dc.subject.otherDyes
dc.subject.otherLinear regression
dc.subject.otherboric acid
dc.subject.otherAdsorption modeling
dc.subject.otherBoric acid–activated carbon
dc.subject.otherIndustry wastes
dc.subject.otherKinetic and isotherm analyze
dc.subject.otherLinear adsorption
dc.subject.otherLinear, pseudo-linear and non-linear adsorption modeling
dc.subject.otherNon linear
dc.subject.otherPhenols removal
dc.subject.otherPseudo linear
dc.subject.otherTea industry waste
dc.subject.otherWaste valorizations
dc.subject.otheraqueous solution
dc.subject.otherisotherm
dc.subject.othermodeling
dc.subject.otherreaction kinetics
dc.subject.otherwaste treatment
dc.subject.otheradsorption kinetics
dc.subject.otherArticle
dc.subject.otheravrami kinetic model
dc.subject.otherchemical interaction
dc.subject.othercontact time
dc.subject.otherdesorption
dc.subject.otherelovich kinetic model
dc.subject.otherenergy dispersive X ray spectroscopy
dc.subject.otherFourier transform infrared spectroscopy
dc.subject.otherfreundlich isotherm model
dc.subject.otherhydrogen bond
dc.subject.otherindustry
dc.subject.otherintraparticle diffusion model
dc.subject.otherkinetic parameters
dc.subject.otherlangmuir isotherm model
dc.subject.otherpH
dc.subject.otherrate constant
dc.subject.otherscanning electron microscopy
dc.subject.othersips isotherm model
dc.subject.othertemperature
dc.subject.otherultraviolet visible spectrophotometry
dc.subject.othervalorization
dc.subject.otherwaste management
dc.subject.otherX ray diffraction
dc.subject.otherX ray photoemission spectroscopy
dc.subject.otherchemistry
dc.subject.otherprocedures
dc.subject.othersewage
dc.subject.otherwater pollutant
dc.titleValorization of tea industry waste into boric acid–activated carbon for phenol removal from aqueous solutions
dc.typeArticle
dspace.entity.typePublication
rdl.citation.openalex1
rdl.citation.scopus1
rdl.citation.wos1
rdl.departmentGümüşhane University, Gümüşhane Vocational School, Department of Chemistry and Chemical Processing Technologies, Gümüşhane, Türkiye
rdl.oa.statusclosed
rdl.sdgSDG12
rdl.sdgSDG06
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)