Näytä suppeat kuvailutiedot

dc.contributor.authorLapinkangas, Suvi
dc.contributor.authorRautio, Lasse
dc.contributor.authorKauppinen, Toni
dc.contributor.authorHu, Tao
dc.contributor.authorPesonen, Janne
dc.contributor.authorLassi, Ulla
dc.date.accessioned2023-01-17T11:25:07Z
dc.date.available2023-01-17T11:25:07Z
dc.date.issued2022
dc.identifier.citationLapinkangas, S., Rautio, L., Kauppinen, T., Hu, T., Pesonen, J., & Lassi, U. (2022). Precipitation of potassium as hazenite from washing water of spent alkaline batteries. <i>Chemical Engineering Journal Advances</i>, <i>12</i>, Article 100426. <a href="https://doi.org/10.1016/j.ceja.2022.100426" target="_blank">https://doi.org/10.1016/j.ceja.2022.100426</a>
dc.identifier.otherCONVID_164973544
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/85063
dc.description.abstractHazenite (KNaMg2(PO4)2 × 14 H2O), a new type of struvite mineral, was precipitated from the potassium-rich washing water of spent alkaline battery black mass. Hazenite can be used as a fertilizer, which would be an additional benefit derived from the sustainable recovery of battery materials. Precipitation experiments were performed using different pH values (9.5–12), Mg:K:PO4 ratios ((1.0–1.5):1:(1.0–1.5)) and temperatures (10–40 °C). Based on the results, hazenite precipitated in a wide pH range under alkaline conditions. The precipitation kinetics were fast, and the purity of the hazenite was high. Overall, hazenite can be precipitated at room temperature without the addition of excess chemicals, which minimizes the consumption of chemicals and energy.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherElsevier BV
dc.relation.ispartofseriesChemical Engineering Journal Advances
dc.rightsCC BY-NC-ND 4.0
dc.subject.otherstruvite
dc.subject.otherhazenite
dc.subject.otherprecipitation
dc.subject.otheralkaline battery
dc.subject.otherblack mass
dc.subject.otherfertilizer
dc.titlePrecipitation of potassium as hazenite from washing water of spent alkaline batteries
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-202301171365
dc.contributor.laitosKokkolan yliopistokeskus Chydeniusfi
dc.contributor.laitosKokkola University Consortium Chydeniusen
dc.contributor.oppiaineSoveltavan kemian yksikköfi
dc.contributor.oppiaineThe Unit of Applied Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn2666-8211
dc.relation.volume12
dc.type.versionpublishedVersion
dc.rights.copyright© 2022 The Authors. Published by Elsevier B.V.
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.subject.ysosähkö- ja elektroniikkaromu
dc.subject.ysofosfaatit
dc.subject.ysokiertotalous
dc.subject.ysosaostus
dc.subject.ysoparistot
dc.subject.ysomineraalit
dc.subject.ysofosforilannoitteet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p21194
jyx.subject.urihttp://www.yso.fi/onto/yso/p8696
jyx.subject.urihttp://www.yso.fi/onto/yso/p28601
jyx.subject.urihttp://www.yso.fi/onto/yso/p10304
jyx.subject.urihttp://www.yso.fi/onto/yso/p2307
jyx.subject.urihttp://www.yso.fi/onto/yso/p2368
jyx.subject.urihttp://www.yso.fi/onto/yso/p14792
dc.rights.urlhttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.relation.doi10.1016/j.ceja.2022.100426
jyx.fundinginformationThis research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
dc.type.okmA1


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