Preparation method of microorganism active tobacco seedling growing base material
A technology of microbial activity and seedling-raising substrates, which is applied in the field of preparation of microbial-active tobacco seedling-raising substrates, can solve the problems of cumbersome process, loss of fertilizer nutrients, and long fermentation time, and achieve large specific surface area, promotion of proliferation, adsorption and anti-decomposition powerful effect
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Embodiment 1
[0036] like figure 1 Shown, the preparation method of microbial activity tobacco seedling culture substrate comprises the following steps:
[0037] Description of raw materials, EM bacteria freeze-dried powder, peat, vermiculite, perlite, brown sugar, salt, urea, rapeseed cake, rice bran, wheat bran, superphosphate and biochar can all be selected from common commercial products, rapeseed The fresher the cake, rice bran and wheat bran, the better; the humus soil should be taken from unpolluted mountain forests with well-preserved ecological vegetation, aired in the shade until semi-dry, and crushed into fine particles no larger than the size of soybeans.
[0038] 1) Activation of EM bacteria: for the first round of activation of EM bacteria, add 500ml of water, 50g of brown sugar, 1.5g of table salt, and 2.5g of urea into a 500ml Erlenmeyer flask, dissolve and bandage, sterilize at 115°C for 20 minutes, take it out, and cool to room temperature. Insert 5g of preserved EM bacte...
Embodiment 2
[0043] A preparation method for microbially active tobacco seedling-growing matrix, comprising the following steps:
[0044] 1) Activation of EM bacteria: For the first round of activation of EM bacteria, add 500ml of water, 40g of brown sugar, 2.5g of salt, and 1.5g of urea into a 500ml Erlenmeyer flask, dissolve and wrap, sterilize at 115°C for 20 minutes, take it out, and cool to room temperature. Insert 2.6g of preserved freeze-dried powder of EM bacteria, and culture at 35°C for 24 hours; for the second round of activation of EM bacteria, add 12L of water, 800g of brown sugar, 10g of salt, and 80g of urea to the serum bottle, dissolve, seal, and sterilize at 115°C for 20 Minutes, take it out, cool to room temperature, insert 32ml of EM bacteria in the first round of activated bacterial liquid, and incubate at 35°C for 3 days; in the third round of EM bacteria activation, mix wheat bran and rice bran at a mass ratio of 1:2, and mix each 5 kg of mixed material Add 100g of b...
Embodiment 3
[0049] A preparation method for microbially active tobacco seedling-growing matrix, comprising the following steps:
[0050] 1) Activation of EM bacteria: for the first round of activation of EM bacteria, add 300ml of water, 60g of brown sugar, 0.5g of salt, and 4g of urea into a 500ml Erlenmeyer flask, dissolve, wrap up, sterilize at 115°C for 20 minutes, take it out, cool to room temperature, and then Add 12g of preserved EM bacteria freeze-dried powder, culture at 35°C for 48 hours; the second round of EM bacteria activation, add 6L of water, 1200g of brown sugar, 50g of salt, and 30g of urea into the serum bottle, dissolve, seal, and sterilize at 115°C for 20 minutes. Take it out, cool to room temperature, insert 80ml of EM bacteria in the first round of activated bacterial liquid, and incubate at 35°C for 3 days; in the third round of EM bacteria activation, mix wheat bran and rice bran at a mass ratio of 2:1, and add brown sugar to every 5 kg of the mixture 100g, 3g salt...
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