TY - JOUR
T1 - Harvesting of microalgae Desmodesmus sp. F51 by bioflocculation with bacterial bioflocculant
AU - Ndikubwimana, Theoneste
AU - Zeng, Xianhai
AU - Liu, Yu
AU - Chang, Jo Shu
AU - Lu, Yinghua
N1 - Funding Information:
This research project was financially supported by the Special Fund for Fujian Ocean High-Tech Industry Development ( 2013015 ). Theoneste Ndikubwimana gratefully acknowledges the Xiamen University and China Scholarship Council for the support. The authors are grateful to Dr. Ching-Nen Nathan Chen in the Institute of Marine Biology, National Sun Yat-sen University (Taiwan, ROC) for providing the microalgae strain. We thank Prof. Ning He (Department of Chemical and Biochemical Engineering, Xiamen University) for providing the cultivation facilities for bacterial bioflocculant. Moreover, the authors acknowledge Prof. Lu Lin (College of Energy, Xiamen University) and Dr. Michael K. Danquah (Department of Chemical & Petroleum Engineering, Curtin University, Malaysia) for their manuscript refining.
Publisher Copyright:
© 2014 Elsevier B.V.
PY - 2014/10/1
Y1 - 2014/10/1
N2 - The small particulate size of microalgae cells and the extremely dilute concentrations of microalgae cultures continue to be major challenges to effective harvesting. In an attempt to find a cost-effective and environmentally friendly harvesting technique, the bioflocculant poly (γ-glutamic acid) (γ-PGA) produced by Bacillus licheniformis CGMCC 2876 was used to concentrate freshwater microalgae Desmodesmus sp. F51. Experimental results showed that the flocculation efficiency was dependent on the initial culture pH. The flocculation efficiency increased from 43.8 ± 1.6% to 98.2 ± 0.1% when the initial culture pH was changed from ~ 7.2, as the original culture pH, to 3. With the optimum operating parameters of bioflocculant dosage of 2.5. mL/L, flash mixing rate of 150. rpm for 1. min, and slow mixing rate of 80. rpm for 2. min, a flocculation efficiency of 99% was achieved. Microscopic photos of the harvested microalgae cells showed no cell damage and hence no premature release of intracellular contents during the process. The bioflocculation process is easy to operate, cost-efficient, environmentally friendly and as effective as chemical flocculation processes applied industrially. The γ-PGA bioflocculant produced by B. licheniformis CGMCC 2876 demonstrated high performance for optimal microalgae recovery and can be applied in commercial-scale microalgae harvesting.
AB - The small particulate size of microalgae cells and the extremely dilute concentrations of microalgae cultures continue to be major challenges to effective harvesting. In an attempt to find a cost-effective and environmentally friendly harvesting technique, the bioflocculant poly (γ-glutamic acid) (γ-PGA) produced by Bacillus licheniformis CGMCC 2876 was used to concentrate freshwater microalgae Desmodesmus sp. F51. Experimental results showed that the flocculation efficiency was dependent on the initial culture pH. The flocculation efficiency increased from 43.8 ± 1.6% to 98.2 ± 0.1% when the initial culture pH was changed from ~ 7.2, as the original culture pH, to 3. With the optimum operating parameters of bioflocculant dosage of 2.5. mL/L, flash mixing rate of 150. rpm for 1. min, and slow mixing rate of 80. rpm for 2. min, a flocculation efficiency of 99% was achieved. Microscopic photos of the harvested microalgae cells showed no cell damage and hence no premature release of intracellular contents during the process. The bioflocculation process is easy to operate, cost-efficient, environmentally friendly and as effective as chemical flocculation processes applied industrially. The γ-PGA bioflocculant produced by B. licheniformis CGMCC 2876 demonstrated high performance for optimal microalgae recovery and can be applied in commercial-scale microalgae harvesting.
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U2 - 10.1016/j.algal.2014.09.004
DO - 10.1016/j.algal.2014.09.004
M3 - Article
AN - SCOPUS:84920658979
VL - 6
SP - 186
EP - 193
JO - Algal Research
JF - Algal Research
SN - 2211-9264
IS - PB
ER -