Application of rabdosia amethystoides as water-blooming cyanobacteria growth inhibitor
A technology of growth inhibitor and bloom cyanobacteria, which is applied in the application field of fragrant tea plant as a bloom cyanobacteria growth inhibitor, can solve the problems of less natural distribution of aquatic plants, poor timeliness of inhibiting algae, and inability of aquatic plants to survive, and achieves the goal of inhibiting the growth of algae. The effect of algae is lasting and stable, ensuring normal growth and good inhibitory effect
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Embodiment 1
[0024] A preparation method for the growth inhibitor of fragrant tea vegetable bloom cyanobacteria, the steps are as follows:
[0025] ⑴ Precisely weigh 5.0g of fragrant tea, put it in a 250mL volumetric flask, add 150mL of distilled water for ultrasonic extraction for 30min, then add 100mL of distilled water, and extract overnight in the dark. spare.
[0026] (2) Prepare the mother liquor of fragrant tea and vegetables into aqueous solutions with different concentration gradients, filter them with a 0.45 μm microporous membrane with water, and add them to the liquid of Microcystis aeruginosa in the logarithmic growth phase, and set up 4 different concentration groups, respectively 0(ck), 5, 25, 100mg / L, each group has 3 parallel samples.
[0027] (3) At 0, 24, 48, 72, 96, 120, 144, and 168 hours, measure the content of chlorophyll a in the algae liquid of each treatment group and the blank control group, respectively. The specific algae inhibition data are shown in Table 1....
Embodiment 2
[0031] A preparation method for the growth inhibitor of fragrant tea vegetable bloom cyanobacteria, the steps are as follows:
[0032] ⑴Precisely weigh 10.0g of fragrant tea, put it in a 500mL volumetric flask, add 300mL of distilled water for ultrasonic extraction for 30min, then add 100mL of distilled water, and extract overnight in the dark. spare.
[0033] (2) Prepare the mother liquor of fragrant tea and vegetables into aqueous solutions with different concentration gradients, filter them with a 0.45 μm microporous membrane with water, and add them to the liquid of Microcystis aeruginosa in the logarithmic growth phase, and set up 4 different concentration groups, respectively 0(ck), 50, 250, 500mg / L, each group has 3 parallel samples.
[0034] (3) At 0, 24, 48, 72, 96, 120, 144, and 168 hours, measure the content of chlorophyll a in the algae liquid of each treatment group and the blank control group, respectively. The specific algae inhibition data are shown in Table ...
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