Skip to main content
Log in

Determining the impacts of fermentative bacteria on wollastonite dissolution kinetics

  • Environmental biotechnology
  • Published:
Applied Microbiology and Biotechnology Aims and scope Submit manuscript

Abstract

Silicate minerals can be a source of calcium and alkalinity, enabling CO2 sequestration in the form of carbonates. For this to occur, the mineral needs to be first dissolved in an acidifying process such as the biological process of anaerobic fermentation. In the present study, the main factors which govern the dissolution process of an alkaline silicate mineral (wollastonite, CaSiO3) in an anaerobic fermentation process were determined. Wollastonite dissolution kinetics was measured in a series of chemical batch experiments in order to be able to estimate the required amount of alkaline silicate that can neutralize the acidifying fermentation process. An anaerobic fermentation of glucose with wollastonite as the neutralizing agent was consequently performed in a fed-batch reactor. Results of this experiment were compared with an abiotic (control) fed-batch reactor in which the fermentation products (i.e. organic acids and alcohols) were externally supplied to the system at comparable rates and proportions, in order to provide chemical conditions similar to those during the biotic (fermentation) experiment. This procedure enabled us to determine whether dissolution of wollastonite was solely enhanced by production of organic acids or whether there were other impacts that fermentative bacteria could have on the mineral dissolution rate. The established pH profiles, which were the direct indicator of the dissolution rate, were comparable in both experiments suggesting that the mineral dissolution rate was mostly influenced by the quantity of the organic acids produced.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Explore related subjects

Discover the latest articles and news from researchers in related subjects, suggested using machine learning.

References

  • Bennett PC, Rogers JR, Choi WJ (2001) Silicates, silicate weathering, and microbial ecology. Geomicrobiol J 18(1):3–19

    Article  CAS  Google Scholar 

  • Berthelin J (1988) Microbial weathering processes in natural environments. In: Lerrnan A, Meybeck M (eds) Physical and chemical weathering in geochemical cycles. Kluwer Academic, Dordrecht

    Google Scholar 

  • Brečević L, Nielsen AE (1989) Solubility of amorphous calcium carbonate. J Cryst Growth 98(3):504–510

    Article  Google Scholar 

  • Datta R, Snyder SW, Richard DD, Henry MP (2010) Biological methane production from coal, manure, sludge, wastes, or other carbonaceous feedstocks with simultaneous sequestration of CO2. United States patent

  • Drever JI, Stillings LL (1997) The role of organic acids in mineral weathering. Colloids Surf, A Physicochem Eng Asp 120(1–3):167–181

    Article  CAS  Google Scholar 

  • Ehrlich HL (1996) How microbes influence mineral growth and dissolution. Chem Geol 132(1–4):5–9

    Article  CAS  Google Scholar 

  • Frey B, Rieder SR, Brunner I, Ploetze M, Koetzsch S, Lapanje A, Brandl H, Furrer G (2010) Weathering-associated bacteria from the Damma Glacier forefield: physiological capabilities and impact on granite dissolution. Appl Environ Microbiol 76(14):4788–4796. doi:10.1128/aem.00657-10

    Article  CAS  Google Scholar 

  • Green E, Luttge A (2006) Incongruent dissolution of wollastonite measured with vertical scanning interferometry. Am Mineral 91(2–3):430–434

    Article  CAS  Google Scholar 

  • Hiebert FK, Bennett PC (1992) Microbial control of silicate weathering in organic-rich ground-water. Science 258(5080):278–281

    Article  CAS  Google Scholar 

  • Huijgen WJJ, Comans RNJ (2005) Carbon dioxide sequestration by mineral carbonation: literature review update 2003–2004. ECN School Fossiel, the Netherlands

  • Icenhower JP, Dove PM (2000) The dissolution kinetics of amorphous silica into sodium chloride solutions: effects of temperature and ionic strength. Geochim Cosmochim Acta 64(24):4193–4203. doi:10.1016/s0016-7037(00)00487-7

    Article  CAS  Google Scholar 

  • Liermann LJ, Barnes AS, Kalinowski BE, Zhou X, Brantley SL (2000) Microenvironments of pH in biofilms grown on dissolving silicate surfaces. Chem Geol 171(1–2):1–16. doi:10.1016/s0009-2541(00)00202-3

    Article  CAS  Google Scholar 

  • Murphy WM, Helgeson HC (1987) Thermodynamic and kinetic constraints on reaction-rates among minerals and aqueous-solutions. 3. Activated complexes and the pH-dependence of the rates of feldspar, pyroxene, wollastonite, and olivine hydrolysis. Geochim Cosmochim Acta 51(12):3137–3153

    Article  CAS  Google Scholar 

  • Pokrovsky OS, Shirokova LS, Benezeth P, Schott J, Golubev SV (2009) Effect of organic ligands and heterotrophic bacteria on wollastonite dissolution kinetics. Am J Sci 309(8):731–772. doi:10.2475/08.2009.05

    Article  CAS  Google Scholar 

  • Rimstidt JD, Dove PM (1986) Mineral solution reaction-rates in a mixed flow reactor—wollastonite hydrolysis. Geochim Cosmochim Acta 50(11):2509–2516

    Article  CAS  Google Scholar 

  • Rogers JR, Bennett PC (2004) Mineral stimulation of subsurface microorganisms: release of limiting nutrients from silicates. Chem Geol 203(1–2):91–108. doi:10.1016/j.chemgeo.2003.09.001

    Article  CAS  Google Scholar 

  • Sand W, Gehrke T, Jozsa P-G, Schippers A (2001) (Bio)chemistry of bacterial leaching—direct vs. indirect bioleaching. Hydrometallurgy 59(2–3):159–175. doi:10.1016/s0304-386x(00)00180-8

    Article  CAS  Google Scholar 

  • Seifritz W (1990) CO2 disposal by means of silicates. Nature 345(6275):486–486

    Article  Google Scholar 

  • Stillings LL, Brantley SL (1995) Feldspar dissolution at 25 °C and pH 3: reaction stoichiometry and the effect of cations. Geochim Cosmochim Acta 59(8):1483–1496. doi:10.1016/0016-7037(95)00057-7

    Article  CAS  Google Scholar 

  • Temudo MF, Kleerebezem R, van Loosdrecht M (2007) Influence of the pH on (open) mixed culture fermentation of glucose: A chemostat study. Biotechnol Bioeng 98(1):69–79

    Google Scholar 

  • Ullman WJ, Kirchman DL, Welch SA, Vandevivere P (1996) Laboratory evidence for microbially mediated silicate mineral dissolution in nature. Chem Geol 132(1–4):11–17

    Article  CAS  Google Scholar 

  • Uroz S, Calvaruso C, Turpault MP, Frey-Klett P (2009) Mineral weathering by bacteria: ecology, actors and mechanisms. Trends Microbiol 17(8):378–387. doi:10.1016/j.tim.2009.05.004

    Article  CAS  Google Scholar 

  • Vandevivere P, Welch SA, Ullman WJ, Kirchman DL (1994) Enhanced dissolution of silicate minerals by bacteria at near-neutral pH. Microb Ecol 27(3):241–251

    Article  CAS  Google Scholar 

  • Weissbart EJ, Rimstidt JD (2000) Wollastonite: incongruent dissolution and leached layer formation. Geochim Cosmochim Acta 64(23):4007–4016

    Article  CAS  Google Scholar 

  • Welch SA, Ullman WJ (1993) The effect of organic acids on plagioclase dissolution rates and stoichiometry. Geochim Cosmochim Acta 57(12):2725–2736

    Article  CAS  Google Scholar 

  • White AF, Brantley SL (1995) Chemical weathering rates of silicate minerals: an overview. Rev Mineral Geochem 31:1–22

    CAS  Google Scholar 

  • White AF, Brantley SL (2003) The effect of time on the weathering of silicate minerals: why do weathering rates differ in the laboratory and field? Chem Geol 202(3–4):479–506. doi:10.1016/j.chemgeo.2003.03.001

    Article  CAS  Google Scholar 

  • Wogelius RA, Walther JV (1991) Olivine dissolution at 25 °C: effects of pH, CO2, and organic acids. Geochim Cosmochim Acta 55(4):943–954

    Article  CAS  Google Scholar 

  • Xie Z, Walther JV (1994) Dissolution stoichiometry and adsorption of alkali and alkaline earth elements to the acid-reacted wollastonite surface at 25 °C. Geochim Cosmochim Acta 58(12):2587–2598. doi:10.1016/0016-7037(94)90130-9

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This research was funded by European Union (Project title: CO2SolStock—Biobased geological CO2 storage, 226306). The authors would like to thank Peter Berkhout at Department of Civil Engineering for allowing us to use his laboratory for preparation of mineral samples. We gratefully acknowledge the help of Professor Hans Geerlings for providing us with sufficient amount of wollastonite. We also gratefully acknowledge Kourosh Honarmand Ebrahimi for his useful comments on the paper.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to S. S. Salek.

Electronic supplementary figures

Below is the link to the electronic supplementary material.

Fig. S1

Cumulative equivalent OH concentration (in molars) obtained from Ca ion released because of wollastonite dissolution vs. equivalent H+ released (in molars) by dissociated organic acids, in the biotic fed batch experiment (a). Cumulative equivalent OH concentration (in molars) obtained from Ca ion released because of wollastonite dissolution vs. equivalent H+ released (in molars) by HCl in the control 2 experiment (b). (DOCX 241 kb)

Fig. S2

The proton dosage rate in the abiotic fed-batch experiment (control 2) which was the same as in the control 1 experiment (DOC 88 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Salek, S.S., Kleerebezem, R., Jonkers, H.M. et al. Determining the impacts of fermentative bacteria on wollastonite dissolution kinetics. Appl Microbiol Biotechnol 97, 2743–2752 (2013). https://doi.org/10.1007/s00253-012-4590-2

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00253-012-4590-2

Keywords