Method for preparing degradable buffer material by using macro fungi mycelia
A technology of cushioning materials and fungi, which is applied in the field of preparation of degradable cushioning materials, can solve the problems of reduced hydraulic properties, poor anti-mildew properties of materials, long preparation time, etc., and achieve excellent cushioning performance and mechanical properties, excellent waterproof and anti-mildew 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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