Rapid malachite green removal from aqueous solution by natural zeolite: Process optimization by response surface methodology

MakaleAçık ErişimScopus SJRQ2
  • SDG 6 · Temiz Su ve Sanitasyon
  • SDG 12 · Sorumlu Üretim ve Tüketim

Özet

In this study, malachite green removal from aqueous solutions by natural zeolite was investigated. The interaction between zeolite and malachite green was determined by SEM/EDX and FTIR. The parameters like adsorbent dosage (0.1–1 mg/100 mL), initial malachite green concentration (40–200 mg/L) and the contact time (10–600 s) were optimized using the central composite design of response surface methodology. Maximum removal yield (99.70%) was obtained at an adsorbent dosage of 0.68 mg/100 mL, an initial malachite green concentration of 79.02 mg/L, and at 414 s contact time. The equilibrium process complied better with the Langmuir isotherm model, which exhibits a single layer adsorption, when compared with the Freundlich isotherm model. Adsorption kinetics followed the pseudo-second-order type kinetic and intra-particle diffusion played an important role onto adsorption mechanism of malachite green. The findings of this study demonstrated that zeolite which is found abundant on earth as a cheap and efficient adsorbent could be used for rapid malachite green adsorption from aqueous solutions.

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https://rdlopen.rawdatalibrary.net/r/munzur/680Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.5004/dwt.2017.20185Yayıncı resmi DOI adresi
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13
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AlanDeğerDil
dc.contributor.authorTanyol, Mehtap
dc.date.accessioned2026-10-28T14:53:31.857014817Z
dc.date.available2026-10-28T14:53:31.857014817Z
dc.date.issued2017
dc.description.abstractIn this study, malachite green removal from aqueous solutions by natural zeolite was investigated. The interaction between zeolite and malachite green was determined by SEM/EDX and FTIR. The parameters like adsorbent dosage (0.1–1 mg/100 mL), initial malachite green concentration (40–200 mg/L) and the contact time (10–600 s) were optimized using the central composite design of response surface methodology. Maximum removal yield (99.70%) was obtained at an adsorbent dosage of 0.68 mg/100 mL, an initial malachite green concentration of 79.02 mg/L, and at 414 s contact time. The equilibrium process complied better with the Langmuir isotherm model, which exhibits a single layer adsorption, when compared with the Freundlich isotherm model. Adsorption kinetics followed the pseudo-second-order type kinetic and intra-particle diffusion played an important role onto adsorption mechanism of malachite green. The findings of this study demonstrated that zeolite which is found abundant on earth as a cheap and efficient adsorbent could be used for rapid malachite green adsorption from aqueous solutions.
dc.description.sponsorshipDepartment of Bioengineering
dc.description.sponsorshipEge Üniversitesi
dc.identifier.doi10.5004/dwt.2017.20185
dc.identifier.eissn1944-3986
dc.identifier.endpage303
dc.identifier.issn1944-3994
dc.identifier.scopus2-s2.0-85020220052
dc.identifier.startpage294
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/munzur/680
dc.identifier.volume65
dc.identifier.wosWOS:000403569200033
dc.language.isoen
dc.publisherDesalination Publications
dc.relation.ispartofDesalination and Water Treatment
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectIsotherm
dc.subjectKinetic
dc.subjectMalachite green
dc.subjectNatural zeolite
dc.subjectResponse surface methodology
dc.subject.classificationEngineering, Chemical
dc.subject.classificationWater Resources
dc.subject.classificationEngineering
dc.subject.otheradsorption
dc.subject.otheraqueous solution
dc.subject.otherdiffusion
dc.subject.othermalachite
dc.subject.otheroptimization
dc.subject.otherreaction kinetics
dc.subject.otherresponse surface methodology
dc.subject.otherzeolite
dc.titleRapid malachite green removal from aqueous solution by natural zeolite: Process optimization by response surface methodology
dc.typeArticle
rdl.citation.openalex13
rdl.citation.scopus12
rdl.citation.wos11
rdl.oa.statushybrid
rdl.oa.urlhttps://doi.org/10.5004/dwt.2017.20185
rdl.scopus.quartileQ2
rdl.sdgSDG06
rdl.sdgSDG12
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)