Aquaculture wastewater contains a huge amount of substances that can cause environmental pollution. However, microalgae can absorb these compounds and convert them into useful biomass. In this study, Chlorella minutissima was grown in the wastewater resulting from saline aquaculture. The microalgae were found to effectively utilize nitrogen and phosphorus in the wastewater for its growth. During wastewater treatment, the cell density increased almost fivefold compared to the initial value (OD680 0.502). Moreover, batch culture resulted in the maximum biomass concentration and productivity of 4.77 g/L and 0.55 g/L/day, respectively. The contents of total nitrogen and total phosphorus in wastewater decreased by 88% and over 99%, respectively. In addition, the content of N-NO3 was reduced by 88.6%, N-NO2 by 74.3%, and dissolved orthophosphates (V) by 99%. At the beginning and throughout the experiment, the content of N-NH4 in wastewater remained below 0.05 mg/L. Furthermore, a high lipid content of 46.4% (w/w) was also obtained from the studied microalgae.
Microalgal biomass and its cellular components are used as substrates for the production of fuels. A valuable group among the components of microalgal biomass is lipids, which act as a precursor for the production of biodiesel in the transesterification process. Some methods, including the creation of stressful conditions, are applied to increase the accumulation of lipids. This study aimed to determine the effect of limited nutrient access on the growth and development of the microalga Chlorella vulgaris and the amount of lipids stored in its cells. Aquaculture wastewater (AWW) was used in the study as a source of nutrients at doses of 20%, 40%, 60%, 80% and 100%. The amount of microalgal biomass, optical density, lipid content after extraction of the biomass in Soxhlet apparatus and chlorophyll a content were determined. It was observed that the microalgae efficiently used the nutrients contained in the AWW. The largest amount of biomass was obtained in AWW80 (727 ± 19.64 mg·L−1). The OD680 (0.492 ± 0.00) determined under the same conditions was almost five times higher in AWW than in the synthetic medium. Under nutrient-stress conditions, the content of lipids in biomass ranged from 5.75% (AWW80) to 11.81% (AWW20). The highest content of chlorophyll a in microalgal cells was obtained in AWW20 (206 ± 11.33 mg∙m−3).
Microalgae are considered to be potentially attractive feedstocks for biodiesel production, mainly due to their fast growth rate and high oil content accumulated in their cells. In this study, the suitability for biofuel production was tested for Chlorella vulgaris, Chlorella fusca, Oocystis submarina, and Monoraphidium strain. The effect of nutrient limitation on microalgae biomass growth, lipid accumulation, ash content, fatty acid profile, and selected physico-chemical parameters of algal biodiesel were analysed. The study was carried out in vertical tubular photobioreactors of 100 L capacity. The highest biomass content at 100% medium dose was found for Monoraphidium 525 ± 29 mg·L−1. A 50% reduction of nutrients in the culture medium decreased the biomass content by 23% for O. submarina, 19% for Monoraphidium, 13% for C. vulgaris and 9% for C. fusca strain. Nutrient limitation increased lipid production and reduced ash content in microalgal cells. The highest values were observed for Oocystis submarina, with a 90% increase in lipids and a 45% decrease in ash content in the biomass under stress conditions. The fatty acid profile of particular microalgae strains was dominated by palmitic, oleic, linoleic, and linoleic acids. Nutrient stress increased the amount of saturated and unsaturated fatty acids affecting the quality of biodiesel, but this was determined by the type of strain.
Fuels and their components accumulate in soil, and many soil organisms are exposed to this pollution. Compared to intensive research on the effect of conventional fuel on soil, very few studies have been conducted on soil ecotoxicity of biofuels. Considering the limited information available, the present study evaluated the changes caused by the presence of biodiesel and diesel fuel in soil. The reaction of higher plants and soil organisms (microbial communities and invertebrates) was analysed. Conventional diesel oil and two types of biodiesel (commercial and laboratory-made) were introduced into the soil. Two levels of contamination were applied—5 and 15% (w/w per dry matter of soil). The plate method was used to enumerate microorganisms from soil contaminated with biodiesel and diesel fuel. Phytotoxicity tests were conducted by a 3-day bioassay based on the seed germination and root growth of higher plant species (Sorghum saccharatum and Sinapis alba). Fourteen-day ecotoxicity tests on earthworm were performed using Eisenia fetida. Based on the results of the conducted tests it was found out that the organisms reacted to the presence of fuels in a diverse manner. As to the microorganisms, both the growth and reduction of their number were noted. The reaction depended on the group of microorganisms, type of fuel and dose of contamination. The lipolytic and amylolytic microorganisms as well as Pseudomonas fluorescens bacteria were particularly sensitive to the presence of fuels, especially biodiesel. Fuels, even at a high dose, stimulated the growth of fungi. Monocotyledonous sugar sorghum plants were more sensitive to the presence of fuels than dicotyledonous white mustard. There was also a significant negative impact of contamination level on plant growth and development. Biodiesel, to a greater extent than conventional fuel, adversely affected the survival and volume of earthworms.
Microalgae are one of the most promising sources of renewable substrates used for energy purposes. Biomass and components accumulated in their cells can be used to produce a wide range of biofuels, but the profitability of their production is still not at a sufficient level. Significant costs are generated, i.a., during the cultivation of microalgae, and are connected with providing suitable culture conditions. This study aims to evaluate the possibility of using sodium bicarbonate as an inexpensive alternative CO2 source in the culture of Chlorella vulgaris, promoting not only the increase of microalgae biomass production but also lipid accumulation. The study was carried out at technical scale using 100 L photobioreactors. Gravimetric and spectrophotometric methods were used to evaluate biomass growth. Lipid content was determined using a mixture of chloroform and methanol according to the Blight and Dyer method, while the carbon content and CO2 fixation rate were measured according to the Walkley and Black method. In batch culture, even a small addition of bicarbonate resulted in a significant (p ≤ 0.05) increase in the amount of biomass, productivity and optical density compared to non-bicarbonate cultures. At 2.0 g∙L–1, biomass content was 572 ± 4 mg·L−1, the maximum productivity was 7.0 ± 1.0 mg·L–1·d–1, and the optical density was 0.181 ± 0.00. There was also an increase in the lipid content (26 ± 4%) and the carbon content in the biomass (1322 ± 0.062 g∙dw–1), as well as a higher rate of carbon dioxide fixation (0.925 ± 0.073 g·L–1·d–1). The cultivation of microalgae in enlarged scale photobioreactors provides a significant technological challenge. The obtained results can be useful to evaluate the efficiency of biomass and valuable cellular components production in closed systems realized at industrial scale.
Biomass of microalgae and the components contained in their cells can be used for the production of heat, electricity, and biofuels. The aim of the presented study was to determine the optimal conditions that will be the most favorable for the production of large amounts of microalgae biomass intended for energy purposes. The study analyzed the effect of the type of lighting, the time of lighting culture, and the pH of the culture medium on the growth of Chlorella vulgaris biomass. The experiment was carried out in vertical tube photobioreactors in three photoperiods: 12/12, 18/6, and 24/0 h (light/dark). Two types of lighting were used in the work: high-pressure sodium light and light-emitting diode. The increase in biomass was determined by the gravimetric method, by the spectrophotometric method on the basis of chlorophyll a contained in the microalgae cells. The number of microalgae cells was also determined with the use of a hemocytometer. The optimal conditions for the production of biomass were recorded at a neutral pH, illuminating the cultures for 18 h a day. The obtained results were 546 ± 7.88 mg·L−1 dry weight under sodium lighting and 543 ± 1.92 mg·L−1 dry weight under light-emitting diode, with maximum biomass productivity of 27.08 ± 7.80 and 25.00 ± 5.1 mg·L−1∙d−1, respectively. The maximum content of chlorophyll a in cells was determined in the 12/12 h cycle and pH 6 (136 ± 14.13 mg∙m−3) under light-emitting diode and 18/6 h, pH 7 (135 ± 6.17 mg∙m−3) under sodium light, with maximum productivity of 26.34 ± 2.01 mg·m−3∙d−1 (light-emitting diode) and 24.21 ± 8.89 mg·m−3∙d−1 (sodium light). The largest number of microalgae cells (2.1 × 106) was obtained at pH 7 and photoperiod of 18/6 h under sodium light, and 12/12 h under light-emitting diode. Based on the results, it can be concluded that the determination of the optimal parameters for the growth and development of microalgae determines the production of their biomass, and such research should be carried out before starting the large-scale production process. In quantifying the biomass during cultivation, it is advantageous to use direct measurement methods.