A method for preparing degradable buffer material using macrofungus mycelium
A buffer material and fungus technology, applied in the field of preparation of degradable buffer materials, can solve the problems of poor anti-mildew resistance, reduced hydraulic properties, long preparation time, etc., and achieve excellent waterproof and anti-mildew properties, excellent buffer properties and mechanical properties Effect
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Embodiment 1
[0026] (1) Preparation of liquid strains
[0027] Select the preferred parent species of Pleurotus eryngii to inoculate into the liquid medium, and shake the flask to cultivate for 3 days with a rotating speed of 200rpm. The female species of Pleurotus eryngii used in the present invention comes from the bacterial strain resource bank of Jiangxi University of Science and Technology, and the number is X613. The female species of Pleurotus eryngii used in the present invention is a PDA medium (potato dextrose agar medium), and its specific formula is : Potato 200g, glucose 20g, agar 20g, potassium dihydrogen phosphate 3g, magnesium sulfate heptahydrate 1.5g, water 1000mL, pH 6.0, the composition of the liquid culture medium that the present invention applies is the sucrose of 3 mass parts, 3 mass parts Number of corn flour, 3 parts by mass of wheat bran, yeast powder of 0.2 parts by mass, potassium dihydrogen phosphate of 0.1 parts by mass, magnesium sulfate heptahydrate of 0.05...
Embodiment 2
[0041] (1) Preparation of liquid strains
[0042] Select the preferred parent species of Pleurotus eryngii to inoculate into the liquid medium, and shake the flask to cultivate for 3 days with a rotating speed of 200rpm. The female species of Pleurotus eryngii used in the present invention comes from the bacterial strain resource bank of Jiangxi University of Science and Technology, and the number is X613. The female species of Pleurotus eryngii used in the present invention is a PDA medium (potato dextrose agar medium), and its specific formula is : Potato 200g, glucose 20g, agar 20g, potassium dihydrogen phosphate 3g, magnesium sulfate heptahydrate 1.5g, water 1000mL, pH 6.0, the composition of the liquid culture medium that the present invention applies is the sucrose of 3 mass parts, 3 mass parts Number of corn flour, 3 parts by mass of wheat bran, yeast powder of 0.2 parts by mass, potassium dihydrogen phosphate of 0.1 parts by mass, magnesium sulfate heptahydrate of 0.05...
Embodiment 3
[0056] (1) Preparation of liquid strains
[0057] Select the preferred parent species of Pleurotus eryngii to inoculate into the liquid medium, and shake the flask to cultivate for 3 days with a rotating speed of 200rpm. The female species of Pleurotus eryngii used in the present invention comes from the bacterial strain resource bank of Jiangxi University of Science and Technology, and the number is X613. The female species of Pleurotus eryngii used in the present invention is a PDA medium (potato dextrose agar medium), and its specific formula is : Potato 200g, glucose 20g, agar 20g, potassium dihydrogen phosphate 3g, magnesium sulfate heptahydrate 1.5g, water 1000mL, pH 6.0, the composition of the liquid culture medium that the present invention applies is the sucrose of 3 mass parts, 3 mass parts Number of corn flour, 3 parts by mass of wheat bran, yeast powder of 0.2 parts by mass, potassium dihydrogen phosphate of 0.1 parts by mass, magnesium sulfate heptahydrate of 0.05...
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