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Synthesis of magnetite from iron-rich mine water using sodium carbonate

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dc.contributor.author Akinwekomi, V
dc.contributor.author Maree, JP
dc.contributor.author Zvinowanda, C
dc.contributor.author Masindi, Vhahangwele
dc.date.accessioned 2017-10-09T07:15:11Z
dc.date.available 2017-10-09T07:15:11Z
dc.date.issued 2017-06
dc.identifier.citation Akinwekomi, V., Maree, JP., Zvinowanda, C. and Masindi, V. 2017. Synthesis of magnetite from iron-rich mine water using sodium carbonate. Journal of Environmental Chemical Engineering, vol 5(3), 2699-2707 en_US
dc.identifier.issn 2213-3437
dc.identifier.uri http://www.sciencedirect.com/science/article/pii/S2213343717302154
dc.identifier.uri http://hdl.handle.net/10204/9642
dc.description Copyright: 2017 Elsevier. Due to copyright restrictions, the attached PDF file only contains the abstract of the full text item. For access to the full text item, please consult the publisher's website. The definitive version of the work is published in Journal of Environmental Chemical Engineering, vol 5(3), 2699-2707 en_US
dc.description.abstract In recent decades, much research has been paying attention on the treatment and desalination of acid mine drainage (AMD) with minimal focus on the recovery of minerals from the resultant residues. Solid sludge produced after the treatment process is highly mineralised and technologies are required for the processing of the final sludge for possible industrial application. Conventionally, magnetite is synthesized using iron-rich, industrial grade chemical reagents making magnetite expensive to produce. This has urged the need to come-up with pragmatic and sustainable technologies of recovering magnetite from waste materials. This has led to the development of the present study which aimed at pre-treating AMD in such a way that magnetite could be generated from the recovered sludge. Synthesis of magnetite nanoparticles was evaluated at varying temperature gradients. The principal mechanism governing the metals recovery was selective precipitation. This was achieved by manipulating the pH and aeration rate of the reaction mixture. Experimental results revealed that optimum conditions that are suitable for the recovery of magnetite nanoparticles from AMD were 2:1 mol ratio of Fe(II)/Fe(III), pH = 10 and temperature ranging from 25 to 100 °C. The purity of synthesized magnetite was 24 (Wt.%) for Al-removed magnetite and 28 (Wt.%) for magnetite synthesized with no Al-removal. Particle size analysis indicated the presence of magnetite nanoparticles having diameters of 0.5 nm. SEM-EDS and mapping revealed the presence of Fe and O on the matrices of synthesized material hence confirming that the recovered material is magnetite. This study successfully proved that magnetite nanoparticles can be synthesized from iron-rich mine drainage. en_US
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.relation.ispartofseries Workflow;19247
dc.subject Magnetite nanoparticles en_US
dc.subject Acid mine drainage en_US
dc.subject Magnetite synthesis en_US
dc.subject Co-precipitation en_US
dc.subject Sodium carbonate en_US
dc.subject Fe-rich mine water en_US
dc.title Synthesis of magnetite from iron-rich mine water using sodium carbonate en_US
dc.type Article en_US
dc.identifier.apacitation Akinwekomi, V., Maree, J., Zvinowanda, C., & Masindi, V. (2017). Synthesis of magnetite from iron-rich mine water using sodium carbonate. http://hdl.handle.net/10204/9642 en_ZA
dc.identifier.chicagocitation Akinwekomi, V, JP Maree, C Zvinowanda, and Vhahangwele Masindi "Synthesis of magnetite from iron-rich mine water using sodium carbonate." (2017) http://hdl.handle.net/10204/9642 en_ZA
dc.identifier.vancouvercitation Akinwekomi V, Maree J, Zvinowanda C, Masindi V. Synthesis of magnetite from iron-rich mine water using sodium carbonate. 2017; http://hdl.handle.net/10204/9642. en_ZA
dc.identifier.ris TY - Article AU - Akinwekomi, V AU - Maree, JP AU - Zvinowanda, C AU - Masindi, Vhahangwele AB - In recent decades, much research has been paying attention on the treatment and desalination of acid mine drainage (AMD) with minimal focus on the recovery of minerals from the resultant residues. Solid sludge produced after the treatment process is highly mineralised and technologies are required for the processing of the final sludge for possible industrial application. Conventionally, magnetite is synthesized using iron-rich, industrial grade chemical reagents making magnetite expensive to produce. This has urged the need to come-up with pragmatic and sustainable technologies of recovering magnetite from waste materials. This has led to the development of the present study which aimed at pre-treating AMD in such a way that magnetite could be generated from the recovered sludge. Synthesis of magnetite nanoparticles was evaluated at varying temperature gradients. The principal mechanism governing the metals recovery was selective precipitation. This was achieved by manipulating the pH and aeration rate of the reaction mixture. Experimental results revealed that optimum conditions that are suitable for the recovery of magnetite nanoparticles from AMD were 2:1 mol ratio of Fe(II)/Fe(III), pH = 10 and temperature ranging from 25 to 100 °C. The purity of synthesized magnetite was 24 (Wt.%) for Al-removed magnetite and 28 (Wt.%) for magnetite synthesized with no Al-removal. Particle size analysis indicated the presence of magnetite nanoparticles having diameters of 0.5 nm. SEM-EDS and mapping revealed the presence of Fe and O on the matrices of synthesized material hence confirming that the recovered material is magnetite. This study successfully proved that magnetite nanoparticles can be synthesized from iron-rich mine drainage. DA - 2017-06 DB - ResearchSpace DP - CSIR KW - Magnetite nanoparticles KW - Acid mine drainage KW - Magnetite synthesis KW - Co-precipitation KW - Sodium carbonate KW - Fe-rich mine water LK - https://researchspace.csir.co.za PY - 2017 SM - 2213-3437 T1 - Synthesis of magnetite from iron-rich mine water using sodium carbonate TI - Synthesis of magnetite from iron-rich mine water using sodium carbonate UR - http://hdl.handle.net/10204/9642 ER - en_ZA


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