A kind of stable cultivation method for indoor simulated algae bloom
A cultivation method and water bloom technology, applied in the field of algae cultivation, can solve the problems of difficulty in capturing the physiological state of algae cells, differences in physiological performance of microalgae in natural water bodies, large errors in research results of microalgae, etc., achieving good application prospects and short cultivation period , low cost effect
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Embodiment 1
[0035] A stable culture method for indoor simulated water blooms, comprising the following steps:
[0036] 1) Collect 1000 mL of water at a depth of 0.5 m from the surface of the Microcystis bloom lake, remove impurities visible to the naked eye, and seal it for later use.
[0037] 2) After collecting natural water and filtering it through a 0.45μm membrane, measure the concentration of TN and TP in it, and then add 0.5mg / mLNaNO to it 3 (as N), 0.05mg / mlKH 2 PO 4 (calculated as P) and pure water, adjust TN to 0.5mg / L, TP to 0.05mg / L, finally high-temperature sterilization, and obtain microalgae culture solution after cooling;
[0038] Inoculate the microalgae obtained in step 1) into 2L of the microalgae culture solution in a sterile environment, and place it in a light incubator for 4 days. 12h: 12h, ventilation 100 ml / min; then the expanded microalgae were centrifuged at 5000rpm for 5min, the supernatant was discarded, and the microalgae culture solution was used to rinse...
Embodiment 2
[0056] A stable culture method for indoor simulated water blooms, comprising the following steps:
[0057] 1) Collect 1000 mL of water at a depth of 0.5 m from the surface of the Microcystis bloom lake, remove impurities visible to the naked eye, and seal it for later use.
[0058] 2) After collecting natural water and filtering it through a 0.45μm membrane, measure the concentration of TN and TP in it, and then add 0.5mg / mLNaNO to it 3 (as N), 0.05mg / mlKH 2 PO 4 (in terms of P) and pure water, adjust TN to 0.5mg / L, TP to 0.05mg / L, and finally high-temperature sterilization, after cooling, the microalgae culture solution is obtained, and then the obtained in step 1) The microalgae were inoculated into 2L of the microalgae culture solution, and placed in a light incubator for 4 days. The culture conditions were 25°C, 2000-2500 lux light, 12h:12h light-to-dark ratio, and 100 ml / min ventilation. Then the expanded microalgae were centrifuged at 5000 rpm for 5 min to discard the...
Embodiment 3
[0062] A stable culture method for indoor simulated water blooms, comprising the following steps:
[0063] 1) Collect 1000 mL of water at a depth of 0.5 m from the surface of the Microcystis bloom lake, remove impurities visible to the naked eye, and seal it for later use.
[0064] 2) After collecting natural water and filtering it through a 0.45μm membrane, measure the concentration of TN and TP in it, and then add 0.5mg / mLNaNO to it 3 (as N), 0.05mg / mlKH 2 PO 4 (in terms of P) and pure water, adjust TN to 0.5mg / L, TP to 0.05mg / L, and finally high-temperature sterilization, after cooling, the microalgae culture solution is obtained, and then the obtained in step 1) The microalgae were inoculated into 2L of the microalgae culture solution, and placed in a light incubator for 4 days. The culture conditions were 25°C, 2000-2500 lux light, 12h:12h light-to-dark ratio, and 100 ml / min ventilation. Then the expanded microalgae were centrifuged at 5000 rpm for 5 min to discard the...
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