Method for extracting microalga oil under assistance of carbonate and absorbing carbon dioxide for circulated culture
A carbon dioxide, assisted extraction technology, applied in microorganism-based methods, biochemical equipment and methods, microorganisms, etc., can solve the problems of increased spray drying cost and energy loss, increased environmental pressure, low extraction efficiency, etc., to achieve energy consumption. The effect of reducing, reducing energy consumption, simplifying process steps
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Embodiment 1
[0068] Embodiment 1 oil-rich new green algae broken wall
[0069] Inoculate 0.1g / L of oil-rich Neochlorella (The Culture Collection of Algae at the University of Texas at Austin) (UTEX 1185) into a 1L Erlenmeyer flask, place it on a shaker, and inoculate it under an LED lamp with a light intensity of 4500lux Under the plate, the temperature is 25° C. and cultured for 7 days to obtain oil-rich new green algae. The medium used in this example is: https: / / utex.org / products / bristol-medium. Take 100mL oil-rich Neochlorophylla liquid and carry out 20-fold centrifugal concentration (10000r / min, 5min), add deionized water to the 20g / L microalgae concentrate obtained by centrifugation, and make it to a volume of 5mL (that is, the quality of water is regarded as 5g), that is, concentrated 20 times. Add a certain quality of DBU and sodium carbonate powder to it, and react for a period of time under certain temperature conditions to break the wall.
[0070] In this example, the effects...
Embodiment 2
[0079] Embodiment 2 seawater chlorella broken wall
[0080] Inoculate 0.1g / L seawater chlorella (CHI-1, Institute of Oceanology, Chinese Academy of Sciences) into a 1L Erlenmeyer flask, place it on a shaker, and place it under an LED light panel with a light intensity of 4500lux at a temperature of 25°C Cultivate under the condition for 7 days to obtain seawater chlorella. Take 200mL seawater chlorella liquid and carry out 40-fold centrifugal concentration (10000r / min, 5min), and add deionized water to the microalgae concentrate obtained by centrifugation to 5mL volume (that is, the quality of water is regarded as 5g), that is, concentrated 40 times. Add DBU and sodium carbonate powder to the system. The mass ratio of DBU to water is 1:7.5, and the mass ratio of sodium carbonate to water is 1:3. Heating in a constant temperature water bath and reacting at 85° C. for 80 minutes to obtain a mixed liquid of microalgae after wall breaking, and the final wall breaking rate was d...
Embodiment 3
[0082] Embodiment 3 Nannochloropsis broken wall
[0083] Inoculate 0.1g / L Nannochloropsis (chy-1, Institute of Oceanology, Chinese Academy of Sciences) into a 1L Erlenmeyer flask, place it on a shaker, and place it on a shaker under an LED light panel with a light intensity of 4500lux at a temperature of 25°C Under the condition of culturing for 7 days, Nannochloropsis was obtained. Take 400mL Nannochloropsis liquid and carry out 25-fold centrifugal concentration (10000r / min, 5min), add deionized water to the microalgae concentrate obtained by centrifugation at 25g / L and make it to 8mL volume (that is, the quality of water is regarded as 5g), that is, concentrated 25 times. Add DBU and sodium carbonate powder to the system. The mass ratio of DBU to water is 1:7.5, and the mass ratio of sodium carbonate to water is 1:3. Heating in a constant temperature water bath, reacting at 90° C. for 100 min, to obtain a mixed solution of microalgae after wall breaking, and the final wal...
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