Preparation method of non-ironing garment material fabric stiffening agent
A stiffening agent and fabric technology, applied in the field of printing and dyeing auxiliaries, can solve the problems of reduced elasticity, poor washing resistance, easy mildew, etc., and achieve the effect of increased stiffness, good washing resistance, and not easy to mildew
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example 1
[0018] First, inoculate Escherichia coli on the surface of the solid medium with an inoculation amount of 2%, then move the solid medium into a constant temperature incubator, and culture it at a constant temperature for 2 days at a temperature of 35°C, then rinse the surface of the medium with 200mL deionized water , to obtain mycelia suspension, the solid medium is mixed with 10g tryptone, 6g beef extract, 0.6g sodium chloride, 13g agar powder, and 800mL deionized water; then select 30 heads and raise them to the 3rd age Tenebrio molitor larvae were placed in an incubator and starved for 36 hours, then 1 μL of the above-mentioned mycelial suspension was injected into the abdomen of each Tenebrio molitor larvae through a micro-syringe, and then the Tenebrio molitor larvae were fed normally for 36 hours. Remove the forefoot of the larvae, collect the effluent with a capillary tube, transfer the obtained effluent to a centrifuge, and centrifuge for 25 minutes at a speed of 8000r...
example 2
[0021] First, inoculate Escherichia coli on the surface of the solid medium with an inoculation amount of 3%, then move the solid medium into a constant temperature incubator, and culture it at a constant temperature for 2 days at a temperature of 36°C, and then rinse the surface of the medium with 250 mL of deionized water , to get mycelia suspension, the solid medium is mixed with 13g tryptone, 7g beef extract, 0.7g sodium chloride, 14g agar powder and 900mL deionized water; then choose 35 heads to raise to 3 ages Tenebrio molitor larvae were placed in an incubator and starved for 42 hours. Then, 2 μL of the above-mentioned mycelia suspension was injected into the abdomen of each Tenebrio molitor larvae through a micro-syringe, and then the Tenebrio molitor larvae were fed normally for 54 hours. Remove the forefoot of the larvae, collect the effluent with a capillary tube, transfer the obtained effluent to a centrifuge, and centrifuge for 28 minutes at a speed of 9000r / min, d...
example 3
[0024] First, inoculate Escherichia coli on the surface of the solid medium with an inoculation amount of 4%, then move the solid medium into a constant temperature incubator, and culture it at a constant temperature for 3 days at a temperature of 37°C, and then rinse the surface of the medium with 300mL deionized water , to get mycelia suspension, the solid medium is mixed with 15g tryptone, 8g beef extract, 0.8g sodium chloride, 15g agar powder and 1000mL deionized water; select 40 heads to raise to 3 years old Tenebrio molitor larvae were placed in an incubator and starved for 48 hours, then 3 μL of the above-mentioned mycelium suspension was injected into the abdomen of each Tenebrio molitor larvae through a micro-syringe, and then the Tenebrio molitor larvae were normally raised for 72 hours. Remove the forefoot of the larvae, collect the effluent with a capillary tube, then transfer the obtained effluent to a centrifuge, and centrifuge for 30 minutes at a speed of 10,000r...
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