Method for controlling haematococcus pluvialis pests and diseases by using photocatalyst
A technology of Haematococcus pluvialis and photocatalyst, which is applied in the biological field, can solve the problems of large-scale production limitations, particle failure, and difficulty in eradication, and achieve the effect of improving the ability to fight against harmful organisms, low cost, and inhibiting growth
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Embodiment 1
[0021] (1) Add the photocatalyst material whose main component is nano-titanium dioxide into pure water to prepare a photocatalyst solution with a concentration of 10 g / L. Before use, use ultrasonic vibration for 10 minutes to obtain a photocatalyst mother solution with good dispersion, and add it to BG- 11 In the nitrogen-deficiency medium, prepare a medium with a photocatalyst concentration of 100 mg / L.
[0022] (2) Take pure and non-polluting Haematococcus pluvialis algae and inoculate it into the above medium with an initial concentration of 0.5 g / L.
[0023] (3) Place the inoculated medium in an outdoor plastic film photobioreactor for cultivation, under natural light conditions, and pass through the environment containing 1.5% CO 2 The mixed air was used, the pH was controlled at 7.0, the temperature was controlled at 25°C, and cultured for 10 days.
[0024] During the cultivation process, samples were taken every day and observed with a microscope. The results showed t...
Embodiment 2
[0028] (1) Add the photocatalyst material whose main component is nano-titanium dioxide into pure water, prepare a photocatalyst solution with a concentration of 2g / L, and stir it mechanically for 40 minutes before use to obtain a well-dispersed photocatalyst mother solution, and add it to BG- 11 In the nitrogen-deficient medium, prepare a medium with a photocatalyst concentration of 10 mg / L.
[0029] (2) Inoculate the liquid of Haematococcus pluvialis containing harmful organisms (including miscellaneous algae, protozoa, bacteria, and chytrid fungus) into the above-mentioned medium, with a total initial concentration of 0.4g / L.
[0030] (3) After inoculation, place it in an outdoor plastic film photobioreactor for cultivation, under natural light conditions, and pass through the environment containing 1.0% CO 2 The mixed air was used, the pH was controlled at 8.0, the temperature was controlled at 25°C, and cultured for 10 days.
[0031] During the cultivation process, sampl...
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