Simultaneous removal of NH4+, H2PO4- and Ni2+ from aqueous sMark solution by thermally activated combinations of steel converter slag and spent alumina catalyst

dc.contributor.authorKadirova, Zukhra C.
dc.contributor.authorHojamberdiev, Mirabbos
dc.contributor.authorBo, Longli
dc.contributor.authorOkada, Kiyoshi
dc.contributor.buuauthorHojiyev, Rustam
dc.contributor.departmentUludağ Üniversitesi/Mühendislik Fakültesi/Tekstil Mühendisliği Bölümü.tr_TR
dc.contributor.researcheridGCT-0509-2022tr_TR
dc.contributor.scopusid36026524100tr_TR
dc.date.accessioned2023-10-23T07:10:26Z
dc.date.available2023-10-23T07:10:26Z
dc.date.issued2015-12-01
dc.description.abstractIndustrial wastes (spent alumina catalyst and steel converter slag) were utilized to prepare low-cost inorganic sorbents by thermal activation at temperatures ranging from 500 to 1000 degrees C. According to the results of X-ray diffraction analysis, high-temperature thermal activation of mixtures of spent alumina catalyst and steel converter slag in different ratios leads to the formation of new crystalline phases. The Ni2+, H2PO4- and NH4+ sorption properties of the prepared samples were investigated in separate batch experiments, employing initial analyte concentration of 10 mmol L-1. The steel converter slag samples calcined at 500 degrees C and 900 degrees C and the mixed sample (70% spent alumina catalyst and 30% steel converter slag) calcined at 1000 degrees C exhibited maximum ion sorption capacities of 3.56 mmol Ni2+ g(-1), 3.28 mmol H-2 PO4+ g(-1) and 2.21 mmol NH4+ g(-1), respectively. The principal mechanisms of Ni2+ sorption were the substitution of Ca2+ ions by Ni2+ ions, precipitation at high pH and sorption on Fe3O4 and SiO2 surfaces present in the samples. The H2PO4-sorption was due mainly to the formation of calcium phosphates and sorption on Fe2O3 and SiO2 surfaces, whereas the removal of NH4+ involved sorption on Al2O3 surfaces of the prepared samples. The results of the kinetics calculations showed that a second-order kinetic model offers a good fit for the present experimental data. The materials prepared from low-cost industrial wastes in this work have the ability to simultaneously remove NH4+, H-2 PO(4)(-)and Ni2+ ions from aqueous solution.en_US
dc.description.sponsorshipMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)en_US
dc.description.sponsorshipJapan Society for the Promotion of Scienceen_US
dc.identifier.citationKadirova, Z. C. (2015). "Simultaneous removal of NH4+, H2PO4- and Ni2+ from aqueous sMark solution by thermally activated combinations of steel converter slag and spent alumina catalyst". Journal of Water Process Engineering, 8, 151-159.en_US
dc.identifier.endpage159tr_TR
dc.identifier.issn2214-7144
dc.identifier.scopus2-s2.0-84945251233tr_TR
dc.identifier.startpage151tr_TR
dc.identifier.urihttps://doi.org/10.1016/j.jwpe.2015.10.004
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S2214714415300520
dc.identifier.urihttp://hdl.handle.net/11452/34507
dc.identifier.volume8tr_TR
dc.identifier.wos000431388700030tr_TR
dc.indexed.scopusScopusen_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.collaborationYurt dışıtr_TR
dc.relation.journalJournal of Water Process Engineeringen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEngineeringen_US
dc.subjectWater resourcesen_US
dc.subjectIndustrial wasteen_US
dc.subjectSpent alumina catalysten_US
dc.subjectSteel converter slagen_US
dc.subjectThermal activationen_US
dc.subjectIon sorptionen_US
dc.subject.scopusRemoval; Temperature; Sludge charen_US
dc.subject.wosEngineering, environmentalen_US
dc.subject.wosEngineering, chemicalen_US
dc.subject.wosWater resourcesen_US
dc.titleSimultaneous removal of NH4+, H2PO4- and Ni2+ from aqueous sMark solution by thermally activated combinations of steel converter slag and spent alumina catalysten_US
dc.typeArticle

Files

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: