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Biomining of iron-containing nanoparticles from coal tailings

  • Danielle MaassEmail author
  • Morgana de Medeiros Machado
  • Beatriz Cesa Rovaris
  • Adriano Michael Bernardin
  • Débora de Oliveira
  • Dachamir Hotza
Environmental biotechnology
  • 8 Downloads

Abstract

Sulfur minerals originating from coal mining represent an important environmental problem. Turning these wastes into value-added by-products can be an interesting alternative. Biotransformation of coal tailings into iron-containing nanoparticles using Rhodococcus erythropolis ATCC 4277 free cells was studied. The influence of culture conditions (stirring rate, biomass concentration, and coal tailings ratio) in the particle size was investigated using a 23 full factorial design. Statistical analysis revealed that higher concentrations of biomass produced larger sized particles. Conversely, a more intense stirring rate of the culture medium and a higher coal tailings ratio (% w/w) led to the synthesis of smaller particles. Thus, the culture conditions that produced smaller particles (< 50 nm) were 0.5 abs of normalized biomass concentration, 150 rpm of stirring rate, and 2.5% w/w of coal tailings ratio. Composition analyses showed that the biosynthesized nanoparticles are formed by iron sulfate. Conversion ratio of the coal tailings into iron-containing nanoparticles reached 19%. The proposed biosynthesis process, using R. erythropolis ATCC 4277 free cells, seems to be a new and environmentally friendly alternative for sulfur minerals reuse.

Keywords

Biomining Coal tailings Iron sulfate nanoparticle Rhodococcus erythropolis Sulfur minerals 

Notes

Acknowledgments

The authors are grateful to Prof. João Batista Marimon da Cunha of the Federal University of Rio Grande do Sul for accomplishing the Mössbauer spectroscopy analysis. We also acknowledge the LABMASSA/UFSC (Laboratório de Transferência de Massa) for the laboratorial infrastructure. Morgana M. Machado is thankful for her doctoral fellowship provided by CAPES (Coordination for the Improvement of Higher Education Personnel). Danielle Maass acknowledges her postdoctoral fellowship provided by CNPq (National Council for Scientific and Technological Development) under project number 154980/2016-1.

Funding

The São Paulo Research Foundation (FAPESP) with the research grant 2019/07659-4 supports the researcher of Danielle Maass.

Compliance with Ethical Standards

Conflict of Interest

The authors declare that they have no conflict of interest.

Ethical approval

This article does not contain any studies with human participants or animals performed by any of the authors.

References

  1. Almeida É, De Oliveira D, Hotza D (2017) Characterization of silver nanoparticles produced by biosynthesis mediated by Fusarium oxysporum under different processing conditions. Bioprocess Biosyst Eng 40:1291–1303.  https://doi.org/10.1007/s00449-017-1788-9 CrossRefGoogle Scholar
  2. Aggarwal S, Karimi IA, Kilbane II JJ, Lee DP (2012) Roles of sulfite oxidoreductase and sulfite reductase in improving desulfurization by Rhodococcus erythropolis. Mol BioSyst 8(10):2724.  https://doi.org/10.1039/c2mb25127b
  3. Alp İ, Deveci H, Yazıcı EY, Türk T, Süngün YH (2009) Potential use of pyrite cinders as raw material in cement production: results of industrial scale trial operations. J Hazard Mater 166:144–149.  https://doi.org/10.1016/J.JHAZMAT.2008.10.129 CrossRefGoogle Scholar
  4. Bachmann RT, Johnson AC, Edyvean RGJ (2014) Biotechnology in the petroleum industry: an overview. Int. Biodeterior. Biodegrad. 86:225–237CrossRefGoogle Scholar
  5. Barhoumi N, Oturan N, Olvera-Vargas H, Brillas E, Gadri A, Ammar S, Oturan MA (2016) Pyrite as a sustainable catalyst in electro-Fenton process for improving oxidation of sulfamethazine. Kinetics, mechanism and toxicity assessment. Water Res 94:52–61.  https://doi.org/10.1016/J.WATRES.2016.02.042 CrossRefGoogle Scholar
  6. Barrie Johnson D, Hallberg KB (2008) Carbon, iron and sulfur metabolism in acidophilic micro-organisms. In: Advances in microbial physiology. pp 201–255Google Scholar
  7. Bazylinski DA, Frankel RB (2004) Magnetosome formation in prokaryotes. Nat Rev Microbiol 2:217–230.  https://doi.org/10.1038/nrmicro842 CrossRefGoogle Scholar
  8. Bharde A, Wani A, Shouche Y, Joy PA, Prasad BLV, Sastry M (2005) Bacterial aerobic synthesis of nanocrystalline magnetite. J Am Chem Soc. 127:9326–9327.  https://doi.org/10.1021/ja0508469 CrossRefGoogle Scholar
  9. Birla SS, Gaikwad SC, Gade AK, Rai MK (2013) Rapid synthesis of silver nanoparticles from Fusarium oxysporum by optimizing physicocultural conditions. Sci World J. 2013:1–12.  https://doi.org/10.1155/2013/796018 CrossRefGoogle Scholar
  10. Boente C, Sierra C, Martínez-Blanco D, Menéndez-Aguado JM, Gallego JR (2018) Nanoscale zero-valent iron-assisted soil washing for the removal of potentially toxic elements. J Hazard Mater 350:55–65.  https://doi.org/10.1016/j.jhazmat.2018.02.016 CrossRefGoogle Scholar
  11. Borah D, Senapati K (2006) Adsorption of Cd(II) from aqueous solution onto pyrite. Fuel. 85:1929–1934.  https://doi.org/10.1016/j.fuel.2006.01.012 CrossRefGoogle Scholar
  12. Brierley CL, Brierley JA (2013) Progress in bioleaching: part B: applications of microbial processes by the minerals industries. Appl Microbiol Biotechnol 97:7543–7552.  https://doi.org/10.1007/s00253-013-5095-3 CrossRefGoogle Scholar
  13. Choi Y, Park TJ, Lee DC, Lee SY (2018) Recombinant Escherichia coli as a biofactory for various single- and multi-element nanomaterials. Proc Natl Acad Sci U S A 115:5944–5949.  https://doi.org/10.1073/pnas.1804543115 CrossRefGoogle Scholar
  14. Coates J (2006) Interpretation of infrared spectra, a practical approach. EAC 1-18.  https://doi.org/10.1002/9780470027318.a5606
  15. De Carvalho CCCR, Da Fonseca MMR (2004) Solvent toxicity in organic-aqueous systems analysed by multivariate analysis. Bioprocess Biosyst Eng. 26:361–375.  https://doi.org/10.1007/s00449-004-0381-1 CrossRefGoogle Scholar
  16. De Carvalho CCCR, Parreño-Marchante B, Neumann G, Da Fonseca MMR, Heipieper HJ (2005) Adaptation of Rhodococcus erythropolis DCL14 to growth on n-alkanes, alcohols and terpenes. Appl Microbiol Biotechnol. 67:383–388.  https://doi.org/10.1007/s00253-004-1750-z CrossRefGoogle Scholar
  17. De Carvalho CCCR, Wick LY, Heipieper HJ (2009) Cell wall adaptations of planktonic and biofilm Rhodococcus erythropolis cells to growth on C5 to C16 n-alkane hydrocarbons. Appl Microbiol Biotechnol. 82:311–320.  https://doi.org/10.1007/s00253-008-1809-3 CrossRefGoogle Scholar
  18. de Carvalho CCCR, Costa SS, Fernandes P, Couto I, Viveiros M (2014) Membrane transport systems and the biodegradation potential and pathogenicity of genus Rhodococcus. Front Physiol 5:1–13.  https://doi.org/10.3389/fphys.2014.00133 Google Scholar
  19. Evangelou VP (1995) Pyrite oxidation and its control: Solution chemistry, surface chemistry, Acid Mine Drainage (AMD), molecular oxidation mechanisms, microbial role, kinetics, control, ameliorates and limitations, microencapsulation. CRC 293p.  https://doi.org/10.1201/9780203741641
  20. Ferrow EA, Mannerstrand M, Sjöberg B (2005) Reaction kinetics and oxidation mechanisms of the conversion of pyrite to ferrous sulphate: a Mössbauer spectroscopy study. Hyperfine Interact 163:109–119.  https://doi.org/10.1007/s10751-005-9200-6 CrossRefGoogle Scholar
  21. Gong Y, Gai L, Tang J, Fu J, Wang Q, Zeng EY (2017) Reduction of Cr(VI) in simulated groundwater by FeS-coated iron magnetic nanoparticles. Sci Total Environ. 595:743–751.  https://doi.org/10.1016/j.scitotenv.2017.03.282 CrossRefGoogle Scholar
  22. Guo J, Guo J, Xu Z (2009) Recycling of non-metallic fractions from waste printed circuit boards: a review. J Hazard Mater 168:567–590.  https://doi.org/10.1016/J.JHAZMAT.2009.02.104 CrossRefGoogle Scholar
  23. Gupta N, Roychoudhury PK, Deb JK (2005) Biotechnology of desulfurization of diesel: prospects and challenges. Appl. Microbiol. Biotechnol. 66:356–366CrossRefGoogle Scholar
  24. Husseiny SM, Salah TA, Anter HA (2015) Biosynthesis of size controlled silver nanoparticles by Fusarium oxysporum, their antibacterial and antitumor activities. Beni-Suef Univ J Basic Appl Sci 4:225–231.  https://doi.org/10.1016/J.BJBAS.2015.07.004 CrossRefGoogle Scholar
  25. IEA (2017) Coal 2017: Analysis and forecasts to 2022. IEA Publications, International Energy Agency. https://www.iea.org/Textbase/npsum/coal2017MRSsum.pdf. Accessed 10 June 2018
  26. Johnson DB (2014) Biomining-biotechnologies for extracting and recovering metals from ores and waste materials. Curr Opin Biotechnol 30:24–31.  https://doi.org/10.1016/j.copbio.2014.04.008 CrossRefGoogle Scholar
  27. Klein C, Hurlbut CS (1993) Manual of mineralogy: (after James D. Dana), 21st edn. Wiley, New York, pp 1813–1895Google Scholar
  28. Krishnamurthy S, Esterle A, Sharma NC, Sahi SV (2014) Yucca-derived synthesis of gold nanomaterial and their catalytic potential. Nanoscale Res Lett. 9:627.  https://doi.org/10.1186/1556-276X-9-627 CrossRefGoogle Scholar
  29. Kundu D, Hazra C, Chatterjee A, Chaudhari A, Mishra S (2014) Extracellular biosynthesis of zinc oxide nanoparticles using Rhodococcus pyridinivorans NT2: multifunctional textile finishing, biosafety evaluation and in vitro drug delivery in colon carcinoma. J Photochem Photobiol B Biol. 140:194–204.  https://doi.org/10.1016/j.jphotobiol.2014.08.001 CrossRefGoogle Scholar
  30. Labiadh L, Oturan MA, Panizza M, Hamadi NB, Ammar S (2015) Complete removal of AHPS synthetic dye from water using new electro-fenton oxidation catalyzed by natural pyrite as heterogeneous catalyst. J Hazard Mater 297:34–41.  https://doi.org/10.1016/J.JHAZMAT.2015.04.062 CrossRefGoogle Scholar
  31. Lang C, Schüler D (2006) Biogenic nanoparticles: production, characterization, and application of bacterial magnetosomes. J Phys Condens Matter. 18:S2815–S2828.  https://doi.org/10.1088/0953-8984/18/38/S19 CrossRefGoogle Scholar
  32. Lee H, Purdon AM, Chu V, Westervelt RM (2004) Controlled assembly of magnetic nanoparticles from magnetotactic bacteria using microelectromagnets arrays. Nano Lett. 4:995–998.  https://doi.org/10.1021/nl049562x CrossRefGoogle Scholar
  33. Lovley DR, Giovannoni SJ, White DC, Champine JE, Phillips EJP, Gorby YA, Goodwin S (1993) Geobacter metallireducens gen. nov. sp. nov., a microorganism capable of coupling the complete oxidation of organic compounds to the reduction of iron and other metals. Arch Microbiol. 159:336–344.  https://doi.org/10.1007/BF00290916 CrossRefGoogle Scholar
  34. Maass D, Valério A, Lourenço LA, de Oliveira D, Hotza D (2019) Biosynthesis of iron oxide nanoparticles from mineral coal tailings in a stirred tank reactor. Hydrometallurgy 184:199–205.  https://doi.org/10.1016/J.HYDROMET.2019.01.010 CrossRefGoogle Scholar
  35. Mahmoud A, Cézac P, Hoadley AFA, Contamine F, D’Hugues P (2017) A review of sulfide minerals microbially assisted leaching in stirred tank reactors. Int Biodeterior Biodegrad 119:118–146.  https://doi.org/10.1016/j.ibiod.2016.09.015 CrossRefGoogle Scholar
  36. Majzlan J, Alpers CN, Koch CB, McCleskey RB, Myneni SCB, Neil JM (2011) Vibrational, X-ray absorption, and Mössbauer spectra of sulfate minerals from the weathered massive sulfide deposit at Iron Mountain, California. Chem Geol. 284:296–305.  https://doi.org/10.1016/j.chemgeo.2011.03.008 CrossRefGoogle Scholar
  37. Narayanan KB, Sakthivel N (2010) Biological synthesis of metal nanoparticles by microbes. Adv. Colloid Interface Sci. 156:1–13CrossRefGoogle Scholar
  38. Oliveira CM, Machado CM, Duarte GW, Peterson M (2016) Beneficiation of pyrite from coal mining. J Clean Prod 139:821–827.  https://doi.org/10.1016/j.jclepro.2016.08.124 CrossRefGoogle Scholar
  39. Peng Z, Xiong C, Wang W, Tan F, Xu Y, Wang X, Qiao X (2017) Facile modification of nanoscale zero-valent iron with high stability for Cr(VI) remediation. Sci Total Environ. 596-597:266–273.  https://doi.org/10.1016/j.scitotenv.2017.04.121 CrossRefGoogle Scholar
  40. Roh Y, Liu SV, Li G, Huang H, Phelps TJ, Zhou J (2002) Isolation and characterization of metal-reducing Thermoanaerobacter strains from deep subsurface environments of the Piceance Basin. Colorado. Appl Environ Microbiol. 68:6013–6020.  https://doi.org/10.1128/AEM.68.12.6013-6020.2002 CrossRefGoogle Scholar
  41. Todescato D, Maass D, Mayer DA, Vladimir Oliveira J, de Oliveira D, Ulson de Souza SMAG, Ulson de Souza AA (2017) Optimal production of a Rhodococcus erythropolis ATCC 4277 Biocatalyst for biodesulfurization and biodenitrogenation applications. Appl Biochem Biotechnol. 183:1375–1389.  https://doi.org/10.1007/s12010-017-2505-5 CrossRefGoogle Scholar
  42. Webmineral (2018) Rhomboclase. http://webmineral.com/data/Rhomboclase.shtml#.WnmeFKinHIU. Accessed 6 Feb 2018
  43. Wynter CI, May L, Oliver FW, Hall JA, Hoffman EJ, Kumar A, Christopher L (2004) Correlation of coal calorific value and sulphur content with 57 Fe Mössbauer spectral absorption. Hyperfine Interact 153:147–152CrossRefGoogle Scholar
  44. Xie Y, Xie S, Chen X, Gui W, Yang C, Caccetta L (2015) An integrated predictive model with an on-line updating strategy for iron precipitation in zinc hydrometallurgy. Hydrometallurgy 151:62–72.  https://doi.org/10.1016/J.HYDROMET.2014.11.004 CrossRefGoogle Scholar
  45. Zhang WX (2003) Nanoscale iron particles for environmental remediation: an overview. J. Nanoparticle Res. 5:323–332.  https://doi.org/10.1023/A:1025520116015 CrossRefGoogle Scholar

Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2019

Authors and Affiliations

  1. 1.Institute of Science and Technology (ICT)Federal University of São Paulo (UNIFESP)São José dos CamposBrazil
  2. 2.Department of Chemical and Food Engineering (EQA)Federal University of Santa Catarina (UFSC)FlorianópolisBrazil
  3. 3.Department of Materials Engineering (PPGCEM)Universidade do Extremo Sul de Santa Catarina (UNESC)CriciúmaBrazil

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