Method for preparing low-carbon alkene by catalytic cracking of micro algae
A low-carbon olefin, catalytic cracking technology, applied in chemical instruments and methods, organic chemistry, hydrocarbons, etc., can solve the problem of no public report on the production of olefins by microalgae
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Embodiment 1
[0029] Embodiment 1: Microalgae cultivation
[0030] Seawater golden algae cultivation:
[0031] Filter natural seawater with ten layers of gauze, sterilize at 121°C for 15 minutes, cool to room temperature, add f / 2 medium to obtain seawater microalgae culture nutrient solution, the specific concentration of each component is as follows: NaNO 3 (sodium nitrate) 8.83×10 -4 M, NaH 2 PO 4 (sodium dihydrogen phosphate) 3.63×10 -5 M, Na 2 SiO 3 (sodium silicate) 1.07×10 -4 M, FeCl 3 (ferric chloride) 1×10 -5 M, EDTA.2Na (EDTA disodium salt) 1×10 -5 M, CuSO 4 (copper sulfate) 4×10 -8 M, Na 2 MoO 4 (sodium molybdate) 3×10 -8 M, ZnSO 4 (zinc sulfate) 8×10 -8 M, CoCl 2 ·6H 2 O(cobalt chloride) 5×10 -8 M, MnCl 2 4H 2 O (manganese chloride) 9×10 -7 M, B 12 1×10 -10 M, B 1 3×10 -7 M, biotin 2 x 10 -9 M.
[0032] The golden algae cells to be cultured were divided into 1.0×10 6Cells / ml were inoculated into the plate reactor equipped with the above nutrient solut...
Embodiment 2
[0033] Embodiment 2: Microalgae cultivation
[0034] Seawater diatom culture:
[0035] Filter natural seawater with ten layers of gauze, sterilize at 121°C for 15 minutes, cool to room temperature, add f / 2 medium to obtain seawater microalgae culture nutrient solution, the specific concentration of each component is as follows: NaNO 3 (sodium nitrate) 8.83×10 -4 M, NaH 2 PO 4 (sodium dihydrogen phosphate) 3.63×10 -5 M, Na 2 SiO 3 (sodium silicate) 1.07×10 -4 M, FeCl 3 (ferric chloride) 1×10 -5 M, EDTA.2Na (EDTA disodium salt) 1×10 -5 M, CuSO 4 (copper sulfate) 4×10 -8 M, Na 2 MoO 4 (sodium molybdate) 3×10 -8 M, ZnSO 4 (zinc sulfate) 8×10 -8 M, CoCl 2 ·6H 2 O(cobalt chloride) 5×10 -8 M, MnCl 2 4H 2 O (manganese chloride) 9×10 -7 M, B 12 1×10 -10 M, B 1 3×10 -7 M, biotin 2 x 10 -9 M.
[0036] The diatom cells to be cultured were divided into 1.0×10 6 Cells / ml were inoculated into the plate reactor equipped with the above nutrient solution, cultured u...
Embodiment 3
[0037] Embodiment 3: Microalgae cultivation
[0038] Freshwater Chlorella Cultivation:
[0039] Add TAP nutrient salt to triple distilled water, sterilize at 121°C for 15 minutes, and cool to room temperature to obtain freshwater microalgae culture nutrient solution. The composition of each component is as follows (mg / l): NaNO 3 100. NaH 2 PO 4 2H 2 O20, EDTA-Na45, H 3 BO 3 33.6, FeCl 3 ·6H 2 O 1.3, MnCl 2 4H 2 O0.36, ZnCl 2 0.021, CoCl 2 ·6H 2 O 0.02, CuSO 4 ·5H 2 O 0.02, (NH 4 ) 6 MO 7 o 24 4H 2 O0.009.
[0040] The green algae cells to be cultured were divided into 0.6×10 6 Cells / ml were inoculated into the plate reactor equipped with the above nutrient solution, cultured under light in the cultivation room, the temperature was controlled at 25-28°C, and fluorescent lamps with a light intensity of 3000-10000Lx were used to irradiate from both sides of the reactor. The ratio is 14h:10h. After culturing for 8 days, the green algae reaching a certain den...
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