Investigation of microalgae culture by autoflocculation methodologies
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DOI:
https://doi.org/10.15625/1811-4989/17059Abstract
Harvesting of microalgae from their different cultivation media has pointed out challenges in resolving the problems of flocculation. These challenges must be faced with a suitable method for inducing flocculation that avoid or limit the microalgae’s contamination. This study developed the fundamental experiments with a support of chemicals and some bacteria strains inducing the flocculation of Chlorella vulgaris SAG 211-19. Particularly, the determination of minimum content of Mg2+, Ca2+, E. coli ATCC 85922 and Bacillus subtilis MT300405 was effectuated with co-cultivation of microalgae and set up in batch culture in Bold’s Basal Medium. As a result, the adjustment in 25 minutes of 199.2 mg/L CaCl2.2H2O, 50 mg/L KH2PO4, and of 141 mg/L MgSO4.7H2O induced a microalgal settling efficiency of 81% and 70%, respectively. Meanwhile, the perfomance of microalgal removing reached up to 83.6% and 84% by the inoculation into microalgal culture media of a minimum initial cell density of 8.1 ´ 105 CFU/mL of Bacillus subtilis MT300405 and 12 ´ 105 CFU/mL of E. coli ATCC 85922, respectively. The flocculation of microalgal cells by bacterial inoculation did not require a high pH adjustment as in the case of salt addition.