Bio-remediation of sulfuric compounds from the ceramic wastewater using indigenous bacteria and Thiobacillus thioparus
Subject Areas : Microbial BiotechnologyMahtab Taherian 1 , Fatemeh Ardestani 2 , Mehdi Parvini 3
1 - M. Sc., Department of Chemical Engineering, Shahrood Branch, Islamic Azad University, Shahrood, Iran
2 - Associate Professor, Department of Chemical Engineering, Qaemshahr Branch, Islamic Azad University, Qaemshahr, Iran
3 - Assistant Professor, Department of Chemical Engineering, Gas and Petroleum, Semnan University, Semnan, Iran
Keywords: Bioremediation, wastewater, Thiobacillus thioparus, Ceramic industries, Sulfide compounds,
Abstract :
Background & Objectives: Sulfide compounds of ceramic industries wastewater cause water pollution as well as plants and aquatic destruction. This study was aimed to evaluate sulfide compounds removal from ceramic industries wastewater by Thiobacillus thioparus and indigenous wastewater bacterial isolates. Materials & Methods: Indigenous bacterial strains were proliferated at pH of 7, the temperature of 25oC, agitation speed of 200 rpm and an aeration rate of 100 mL min-1 in a 2 L bioreactor for 15 consecutive cycles. Sulfide compounds removal function of T. thioparus and indigenous bacterial strains along with the effect of pH and initial sulfide concentrations were investigated. Results: The results showed a thiosulfate removal rate of 250 mg sulfide L-1 h-1, a thiosulfate conversion percentage of 100% and a thiosulfate oxidation time of 44 min following 8 consecutive cycles. The sulfide removal rate of T. thioparus and ceramic wastewater indigenous bacteria was obtained as 246.5 and 276.5 mg sulfide L-1 h-1, respectively. Sulfide removal rate by proliferated bacteria decreased from 250 at pH of 7 to 230 and 180 mg sulfide L-1 h-1 at pH of 8 and 9, respectively. Bacterial isolates had an acceptable function in sulfide concentration of 3000 mg L-1, as well. Sulfide removal ability of T. thioparus isolates was decreased by 2.5 and 4 folds, when pH changed from 7 to 8 and 9, respectively. This bacterial strain was not able to tolerate high sulfide concentrations. Conclusion: The results showed that bacteria isolated from ceramic industries wastewater have a higher capability of sulfide compounds removal as compared to T. thioparus isolates.
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81(4): 765-770.
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P, Khodaparast Z, Kamali M, Elliott A. Wastewater treatment and reclamation: A review of pulp
and paper industry practices and opportunities. Bio Res. 2016; 11(3): 7953-8091.
14. Mojarrad Moghanloo GM. Fatehifar E, Saedy S, Aghaeifar Z, Abbasnezhad H. Biological
oxidation of hydrogen sulfide in mineral media using a biofilm airlift suspension reactor.
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[In Persian]
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18. Oyarzun P, Arancibia F, Canales Ch, E. Aroca G. Biofiltration of high concentration of
hydrogen sulphide using Thiobacillus thioparus. Process Biochem. 2003; 39(2): 165-170.
19. Swamy N, Prashanth KN, Basavaiah K. Titrimetric and spectrophotometric assay of
diethylcarbamazine citrate in formulations using iodate and iodide mixture as reagents. Braz J
Pharm Sci. 2015; 51(1): 43-52.
20. Beard S, Paradela A, Albar JP, Jerez CA. Growth of Acidithiobacillus ferrooxidans ATCC
23270 in thiosulfate under oxygen-limiting conditions generates extracellular sulfur globules by
means of a secreted tetrathionate hydrolase. Front Microbiol. 2011; 2: 79.
21. Kolmert A, Wikstrom P, Hallberg KB. A fast and simple turbidimetric method for the
determination of sulfate in sulfate-reducing bacterial cultures. J Microbiol Methods. 2000; 41(3):
179-184.
_||_
sulphur compounds through biotrickling filters connected in series: Effect of H2S. Electron J
Biotechnol. 2012; 15(3): 1-15.
2. Tang K, Baskaran V, Nemati M. Bacteria of the sulphur cycle: An overview of microbiology,
biokinetics and their role in petroleum and mining industries. Biochem Eng J. 2009; 44(1):
73-94.
3. Mahmood Q, Zheng P, Cai J, Hayat Y, Hassan MJ, Wu DL, Hu BL. Sources of sulfide in waste
streams and current biotechnologies for its removal. J Zhejiang Univ-Sc A. 2007; 8: 1126-1140.
4. Zytoon MAM, Alzahrani AA, Noweir MH, EL-Marakby FA. Bioconversion of high
concentrations of hydrogen sulfide to elemental sulfur in airlift bioreactor. Sci World J. 2014;
2014: 675673.
5. Zain WSMd, Salleh NIH, Abdullah A. Natural biocides for mitigation of sulphate reducing
bacteria. Int J Corrosion. 2018; 2: 1-7.
6. Ramirez M, Fernandez M, Granada C, Le Borgne S, Gomez JM, Cantero D. Biofiltration of
reduced sulphur compounds and community analysis of sulphur- oxidizing bacteria. Bioresource
Technol. 2011; 102: 4047-4053.
7. Chung YC, Cheng CY, Chen TY, Hsu JS, Kui CC. Structure of the bacterial community in a
biofilter during dimethyl sulfide (DMS) removal processes. Bioresource Technol. 2010; 101:
7165-7168.
8. Ramirez M, Gomez JM, Aroca G, Cantero D. Removal of hydrogen sulfide by immobilized
Thiobacillus thioparus in a biotrickling filter packed with polyurethane foam. Bioresource
Technol. 2009; 100: 4989-4995.
9. Gonzalez-Sanchez A, Revah S. Biological sulfide removal under alkaline and aerobic conditions
in a packed recycling reactor. Water Sci Technol. 2009; 59(7): 1415-1421.
10. Lohwacharin J, Annachhatre AP. Biological sulfide oxidation in an airlift bioreactor.
Bioresource Technol. 2010; 101(7): 2114-2120.
11. Xiao Hua G, Wei Sheng G. Study on treatment of sulfide wastewater using
adsorption-biological contact oxidation process. Int Symposium Water Resour Environ Protect
(ISWREP), Xian. 2011.
12. Chen C, Wang A, Ren N, Kan H, Lee DJ. Biological breakdown of denitrifying sulfide
removal process in high-rate expanded granular bed reactor. Appl Microbiol Biotechnol. 2008;
81(4): 765-770.
13. Hubbe MA, Metts JR, Hermosilla D, Blanco MA, Yerushalmi L, Haghighat F, Lindholm-Lehto
P, Khodaparast Z, Kamali M, Elliott A. Wastewater treatment and reclamation: A review of pulp
and paper industry practices and opportunities. Bio Res. 2016; 11(3): 7953-8091.
14. Mojarrad Moghanloo GM. Fatehifar E, Saedy S, Aghaeifar Z, Abbasnezhad H. Biological
oxidation of hydrogen sulfide in mineral media using a biofilm airlift suspension reactor.
Bioresource Technol. 2010; 101(21): 8330-8335.
15. Zabihi M, Taran M. Optimization of environmental factors affecting gold microbial
bioleaching by indigenous bacteria in Zarshuran mineral ore. J Microb World. 2017; 10(3):
202-209. [In Persian]
16. Baghi Sefidan H, Tarinejad A. Bioremediation of both mineral and organic mercury via
construction of recombinant vector pET28a (+)-merA-merB. J Microb World. 2018; In Press.
[In Persian]
17. Mohammadzadeh Karkaragh R, Chorom M, Motamedi H, Mohabat A. Biosorption and
bioaccumulation of Cd and Ni in competitive solution by three bacteria isolated from polluted
soils to sewage sludge. J Microb World. 2014; 7(3): 241-251. [In Persian]
18. Oyarzun P, Arancibia F, Canales Ch, E. Aroca G. Biofiltration of high concentration of
hydrogen sulphide using Thiobacillus thioparus. Process Biochem. 2003; 39(2): 165-170.
19. Swamy N, Prashanth KN, Basavaiah K. Titrimetric and spectrophotometric assay of
diethylcarbamazine citrate in formulations using iodate and iodide mixture as reagents. Braz J
Pharm Sci. 2015; 51(1): 43-52.
20. Beard S, Paradela A, Albar JP, Jerez CA. Growth of Acidithiobacillus ferrooxidans ATCC
23270 in thiosulfate under oxygen-limiting conditions generates extracellular sulfur globules by
means of a secreted tetrathionate hydrolase. Front Microbiol. 2011; 2: 79.
21. Kolmert A, Wikstrom P, Hallberg KB. A fast and simple turbidimetric method for the
determination of sulfate in sulfate-reducing bacterial cultures. J Microbiol Methods. 2000; 41(3):
179-184.