A kind of preparation method of continuous sio2 airgel fiber
An aerogel and fiber technology, which is applied in chemical instruments and methods, wet spinning, rayon of inorganic raw materials, etc., can solve the problems of unreported aerogel fibers, achieve good spinnability, cheap raw materials, The effect of easy availability of raw materials
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Embodiment 1
[0032] 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. Use deionized water to replace the solution in the fiber, and freeze-dry to obtain SiO 2 Airgel fibers. The spinning process is very smooth and continuous. Prepared SiO 2 Airgel fiber specific surface area is 565.8m 2 / g, the most probable pore diameter is 10nm. 64% of the maximum adsorption capacity of methylene blue can be ...
Embodiment 2
[0034] 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. Use deionized water to replace the solution in the fiber, and freeze-dry to obtain SiO 2 Airgel fibers. Occasionally, there is a phenomenon of broken filaments during the spinning process. Prepared SiO 2 Airgel fiber specific surface area is 421.6m 2 / g, the most probable pore diameter is 10nm. 59% of the maximum ads...
Embodiment 3
[0036] 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. Use deionized water to replace the solution in the fiber, and freeze-dry to obtain SiO 2 Airgel fibers. Occasionally, there is a phenomenon of broken filaments during the spinning process. Prepared SiO 2 Airgel fiber specific surface area is 435.4m 2 / g, the most probable pore diameter is 11nm. It takes 5 minutes to reach 60% of t...
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