A pvp coated resilient sio 2 Preparation method of airgel fiber
An aerogel and fiber technology, which is applied in fiber processing, fiber chemical characteristics, wet spinning, etc., to achieve the effects of cheap raw materials, expanding the scope of application, and enriching holes
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Embodiment 1
[0033] Sodium water glass with a modulus of 2 and 50 Baume degrees was used as the spinning stock solution, and 0.8 mol / L dilute sulfuric acid solution was used as the coagulation bath to carry out reactive wet spinning. The orthosilicic acid / silicate fiber formed in the coagulation bath was wound at a winding speed of 0.1 m / s. The wound fiber was immersed in 0.005mol / L dilute sulfuric acid for 10 days for aging, so as to realize the transformation from orthosilicic acid / silicate fiber to SiO 2 The fibers are transformed, and a large number of holes are formed at the same time. After aging, the fibers were washed with deionized water until neutral. Solvent replacement was performed with ethanol and dried at normal temperature. After drying, immerse the fiber in 10wt% PVP aqueous solution for 5 minutes, take it out, and repeat the immersion in PVP and drying operations 5 times. Finally, after freeze-drying, a kind of tough SiO coated with PVP is obtained. 2 Airgel fibers. ...
Embodiment 2
[0035] Potassium water glass with a modulus of 3 and 35 degrees Baume was used as the spinning stock solution, and 0.2mol / L dilute sulfuric acid solution was used as the coagulation bath to carry out reactive wet spinning. The orthosilicic acid / sodium silicate fiber formed in the coagulation bath was wound at a winding speed of 0.5 m / s. The wound fiber was immersed in 0.005mol / L dilute sulfuric acid for 10 days for aging, so as to realize the transformation from orthosilicic acid / silicate fiber to SiO 2 The fibers are transformed, and a large number of holes are formed at the same time. After aging, the fibers were washed with deionized water until neutral. Solvent replacement was performed with ethanol and dried at normal temperature. After drying, immerse the fiber in 5wt% PVP aqueous solution for 5 minutes, take it out, and repeat the immersion in PVP and drying operations 4 times. Finally, after freeze-drying, the tough SiO coated with PVP was obtained. 2 Airgel fibers...
Embodiment 3
[0037] Potassium water glass with a modulus of 3 and 35 degrees Baume was used as the spinning stock solution, and 0.8 mol / L dilute sulfuric acid solution was used as the coagulation bath to carry out reactive wet spinning. The orthosilicic acid / potassium silicate fiber formed in the coagulation bath was wound at a winding speed of 1 m / s. The wound fiber was immersed in 0.1mol / L dilute sulfuric acid for 5 days for aging, and the transformation from orthosilicic acid / silicate fiber to SiO 2 The fibers are transformed, and a large number of holes are formed at the same time. After aging, the fibers were washed with deionized water until neutral. Solvent replacement was performed with ethanol and dried at normal temperature. After drying, immerse the fiber in 15wt% PVP aqueous solution for 5 minutes, take it out, and repeat the immersion in PVP and drying operation 3 times. Finally, after freeze-drying, the tough SiO coated with PVP was obtained. 2 Airgel fibers. Prepared du...
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